1-Boc-3-pyrrolidinecarbaldehyde

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1-Boc-3-pyrrolidinecarbaldehyde manufacturers

1-Boc-3-pyrrolidinecarbaldehyde Basic information
Product Name:1-Boc-3-pyrrolidinecarbaldehyde
Synonyms:1-BOC-3-PYRROLIDINECARBALDEHYDE;3-FORMYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;1-BOC-3-FORMYL-PYRROLIDINE;1-BOC-PYRROLIDINE-3-CARBOXALDEHYDE;N-BOC-3-FORMYL PYRROLIDINE;1-boc-3-pyrrolidineearbaldehyde;-Boc-3-pyrrolidinecarbaldehyde;1-Boc-3-formyl-pyrrolidine 95%
CAS:59379-02-1
MF:C10H17NO3
MW:199.25
EINECS:
Product Categories:pharmacetical;Pyrrole&Pyrrolidine&Pyrroline
Mol File:59379-02-1.mol
1-Boc-3-pyrrolidinecarbaldehyde Structure
1-Boc-3-pyrrolidinecarbaldehyde Chemical Properties
Boiling point 276.3±33.0 °C(Predicted)
density 1.148±0.06 g/cm3(Predicted)
refractive index 1.47
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
pka-2.44±0.40(Predicted)
form Oil
color Colourless
InChIInChI=1S/C10H17NO3/c1-10(2,3)14-9(13)11-5-4-8(6-11)7-12/h7-8H,4-6H2,1-3H3
InChIKeyDWLADVOODHZCFV-UHFFFAOYSA-N
SMILESN1(C(OC(C)(C)C)=O)CCC(C=O)C1
CAS DataBase Reference59379-02-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-51-36-22
Safety Statements 26-36/37/39
HazardClass IRRITANT
HS Code 2933998090
MSDS Information
1-Boc-3-pyrrolidinecarbaldehyde Usage And Synthesis
Chemical PropertiesColorless to light yellow oil
Uses1-Boc-pyrrolidine-3-carboxaldehyde is used in the preparation of tertiary amines as agonists of the nuclear hormone receptor Rev-erbα.
Synthesis
1-Boc-3-hydroxymethylpyrrolidine

114214-69-6

1-Boc-3-pyrrolidinecarbaldehyde

59379-02-1

General procedure for the synthesis of 1-Boc-3-pyrrolidinecarboxaldehyde from 1-Boc-3-hydroxymethylpyrrolidine: 1 kg of N-Boc-pyrrolidine-3-methanol was dissolved in 5 liters of dimethylsulfoxide (DMSO), and 2.14 kg of manganese dioxide was slowly added at room temperature. The reaction mixture was stirred at room temperature for about 24 hours to ensure complete reaction. Upon completion of the reaction, insoluble solids were removed by filtration and the filtrate was concentrated by rotary evaporator to remove solvent. Ultimately, N-Boc-pyrrolidine-3-carbaldehyde (920 g) was purified by reduced pressure distillation in 93% yield.

References[1] Patent: CN106588738, 2017, A. Location in patent: Paragraph 0036; 0041; 0042; 0046; 0047; 0048
[2] Patent: WO2005/49602, 2005, A1. Location in patent: Page/Page column 89; 90; 131
[3] Patent: WO2005/49605, 2005, A1. Location in patent: Page/Page column 117; 118; 159
[4] Synlett, 2017, vol. 28, # 4, p. 425 - 428
[5] Bioorganic and medicinal chemistry letters, 2002, vol. 12, # 13, p. 1785 - 1789
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