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4-(Boc-Aminomethyl)piperidine

CAS No.
135632-53-0
Chemical Name:
4-(Boc-Aminomethyl)piperidine
Synonyms
TERT-BUTYL (PIPERIDIN-4-YLMETHYL)CARBAMATE;tert-Butyl N-(piperidin-4-ylmethyl)carbamate;PIP(4-BOC-AM);BUTTPARK 43\57-92;(BOC-4-AMINOMETHYL)PIPERIDINE;4-(BOC-AMINOMETHYL)PIPERIDINE;4-N-BOC-AMINOMETHYL PIPERIDINE;4-(2-BOC-AMINOMETHYL) PIPERIDINE;me: 4-(Boc-Aminomethyl)piperidine;4-(Boc-aminomethyl)piperidine,97%
CBNumber:
CB4102632
Molecular Formula:
C11H22N2O2
Molecular Weight:
214.3
MDL Number:
MFCD01631214
MOL File:
135632-53-0.mol
Last updated:2025-07-24 18:13:46
Product description Number Pack Size Price
4-(tert-Butoxycarbonylaminomethyl)piperidine >98.0%(GC)(T) B4444 1g $344
tert-Butyl(Piperidin-4-ylmethyl)carbamate B701450 1g $75
tert-Butyl (piperidin-4-ylmethyl)carbamate 95+% 016373 5g $48
4-(N-Boc-aminomethyl)piperidine FB36900 2g $50
4-(Boc-aminomethyl)piperidine 97% JK989088 1g $67
More product size

4-(Boc-Aminomethyl)piperidine Properties

Melting point 106 °C
Boiling point 321.8±15.0 °C(Predicted)
Density 0.981±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in DMSO.
pka 12.72±0.46(Predicted)
form powder to crystal
color White to Almost white
CAS DataBase Reference 135632-53-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H314-H318
Precautionary statements  P260h-P301+P330+P331-P303+P361+P353-P305+P351+P338-P405-P501a
Hazard Codes  C,Xi
Risk Statements  34-36/38
Safety Statements  26-36/37/39-45
RIDADR  3259
Hazard Note  Corrosive
HazardClass  IRRITANT
HazardClass  8
PackingGroup 
HS Code  29333990
NFPA 704
1
3 0

4-(Boc-Aminomethyl)piperidine price More Price(29)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical B4444 4-(tert-Butoxycarbonylaminomethyl)piperidine >98.0%(GC)(T) 135632-53-0 1g $344 2025-07-31 Buy
TRC B701450 tert-Butyl(Piperidin-4-ylmethyl)carbamate 135632-53-0 1g $75 2021-12-16 Buy
Matrix Scientific 016373 tert-Butyl (piperidin-4-ylmethyl)carbamate 95+% 135632-53-0 5g $48 2021-12-16 Buy
Biosynth Carbosynth FB36900 4-(N-Boc-aminomethyl)piperidine 135632-53-0 2g $50 2021-12-16 Buy
Frontier Specialty Chemicals JK989088 4-(Boc-aminomethyl)piperidine 97% 135632-53-0 1g $67 2021-12-16 Buy
Product number Packaging Price Buy
B4444 1g $344 Buy
B701450 1g $75 Buy
016373 5g $48 Buy
FB36900 2g $50 Buy
JK989088 1g $67 Buy

4-(Boc-Aminomethyl)piperidine Chemical Properties,Uses,Production

Uses

4-(Boc-aminomethyl)piperidine is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.

Synthesis

4-(Aminomethyl)piperidine

7144-05-0

N-BOC-IMIDAZOLE

49761-82-2

4-(Boc-Aminomethyl)piperidine

135632-53-0

General procedure: 4-aminomethylpiperidine (3.6 g) and 1-BOC-imidazole (5.3 g) were dissolved in toluene (80 mL), and the reaction was stirred at 25°C overnight. After completion of the reaction, the solution was concentrated and the residue was purified by silica gel column chromatography (eluent: EtOAc/hexane=1/2) to afford Intermediate 227-I (4.7 g) in 70% yield. Intermediate 227-I (4.7 g) and triethylamine (2.7 mL) were dissolved in 1-pentanol (20 mL), 2,4-dichloro-6-aminopyrimidine (5.4 g) was added, and the reaction was carried out at 120 °C for 12 hours. After completion of the reaction, the solvent was removed and the residue was purified by silica gel column chromatography (eluent: EtOAc/hexane=1/9) to afford Intermediate 227-II (5.2 g) in 70% yield. Intermediate 227-II (1.0 g) was treated with 1 M HCl (20 mL) in CH2Cl2 (10 mL) and stirred at room temperature for 8 hours. After completion of the reaction, the solution was concentrated, the residue neutralized with NH4OH and extracted with CH2Cl2. The organic layer was separated and concentrated, and the residue was purified by silica gel column chromatography (eluent: MeOH) to afford Intermediate 227-III (636 mg) in 90% yield. Intermediate 222-III (790 mg) was added to a solution of intermediate 227-III (450 mg) in MeOH (20 mL) and stirred at 25 °C for 2 hours. Then NaBH(OAc)3 (2.0 g) was added and the reaction was continued at 25 °C for 12 hours. After completion of the reaction, the solution was concentrated, saturated NaHCO3 solution was added and extracted with CH2Cl2. The organic layer was separated and concentrated, and the residue was purified by silica gel column chromatography (eluent: MeOH) to afford intermediate 227-IV (539 mg) in 60% yield. N1-morpholino-N1-piperazine ethane (240 mg) was added to a 1-pentanol (1 mL) solution of Intermediate 227-IV (160 mg) and stirred at 120 °C for 8 hours. After completion of the reaction, the solution was concentrated and the residue was purified by silica gel column chromatography (eluent: EtOAc/MeOH=5/1) to afford Intermediate 227-V (85 mg) in 40% yield. 20% TFA/CH2Cl2 (1 mL) was added to a solution of CH2Cl2 (1 mL) of intermediate 227-V (85 mg) and stirred at room temperature for 8 hours. After completion of the reaction, the solvent was removed and the residue was purified by silica gel column chromatography (eluent: 21% NH3(aq)/MeOH=1/19) to afford compound 227 (65 mg) in 90% yield. Finally, compound 227 was treated with a solution of CH2Cl2 (1 mL) in 1M HCl (1 mL) for 0.5 hours. After removal of the solvent, the residue was treated with ether and filtered to give the hydrochloride salt of compound 227.CI-MS (M++1): 544.4.

References

[1] Patent: US2006/281712, 2006, A1. Location in patent: Page/Page column 108-109

7144-05-0
49761-82-2
135632-53-0
Synthesis of 4-(Boc-Aminomethyl)piperidine from 4-(Aminomethyl)piperidine and N-BOC-IMIDAZOLE
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View Lastest Price from 4-(Boc-Aminomethyl)piperidine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4-(Boc-Aminomethyl)piperidine pictures 2025-04-04 4-(Boc-Aminomethyl)piperidine
135632-53-0
US $0.00-0.00 / KG 1KG 98% 1ton Henan Aochuang Chemical Co.,Ltd.
4-(Boc-Aminomethyl)piperidine pictures 2022-01-26 4-(Boc-Aminomethyl)piperidine
135632-53-0
US $0.00 / KG 1KG 97.8% 100 tons Honest Joy Holdings Limited
me:	4-(Boc-Aminomethyl)piperidine pictures 2019-09-02 me: 4-(Boc-Aminomethyl)piperidine
135632-53-0
US $1.00 / KG 1KG 98% 1kg; 2kg;10kg; 100kg Career Henan Chemical Co

4-(Boc-Aminomethyl)piperidine Spectrum

4-(2-BOC-AMINOMETHYL) PIPERIDINE 4-AMINOMETHYLPIPERIDINE, BOC PROTECTED 4-(BOC-AMINOMETHYL)PIPERIDINE 4-N-BOC-AMINOMETHYL PIPERIDINE 4-(TERT-BUTYLOXYCARBONYL-AMINOMETHYL)-PIPERIDINE 4-(TERT-BUTOXYCARBONYLAMINOMETHYL)PIPERIDINE 4-(T-BUTYLOXYCARBONYL-AMINOMETHYL)-PIPERIDINE BUTTPARK 43\57-92 (BOC-4-AMINOMETHYL)PIPERIDINE 4-(Aminomethyl)piperidine, 4-BOC protected PIPERIDIN-4-YLMETHYL-CARBAMIC ACID TERT-BUTYL ESTER PIP(4-BOC-AM) TERT-BUTYL N-(4-PIPERIDINYLMETHYL)CARBAMATE tert-butyl n-(4-piperidylmethyl)carbamate TERT-BUTYL (PIPERIDIN-4-YLMETHYL)CARBAMATE me: 4-(Boc-Aminomethyl)piperidine 4-(Aminomethyl)piperidine, 4-BOC protected 95% (BOC-4-aminomethyl)piperidine, min. 95 % Carbamic acid, (4-piperidinylmethyl)-, 1,1-dimethylethyl ester tert-butyl (piperidin-4-ylmethyl)carbamate(SALTDATA: HCl) 4-(Boc-aminomethyl)-piperidine hydrochloride tert-butyl piperidin-4-ylmethylcarbamate hydrochloride 1,1-diMethylethyl [(piperidin-4-yl)Methyl]carbaMate tert-Butyl [(piperidin-4-yl)methyl]carbamate, 4-{[(tert-Butoxycarbonyl)amino]methyl}piperidine 4-(Boc-aminomethyl)piperidine,97% Carbamic acid, N-(4-piperidinylmethyl)-, 1,1-dimethylethyl ester tert-Butyl N-(piperidin-4-ylmethyl)carbamate (4-Piperidylmethyl)carbamic Acid tert-Butyl Ester tert-Butyl (4-Piperidylmethyl)carbamate 5,7-diethyl-2-(3-nitrophenyl)-1,3-diazaadamantan-11-one 4-(Boc-aminomethyl)piperidine - [A12321] 135632-53-0 Pyrans, Piperidines & Piperazines pharmacetical Aminomethyl's Pyrans, Piperidines &Piperazines Piperidine