| Identification | Back Directory | [Name]
1-N-BOC-4-BROMOPIPERIDINE | [CAS]
180695-79-8 | [Synonyms]
1-Boc-4-broMopiperidin
1-Boc-4-bromopiperidine
N-BOC-4-BROMO-PIPERIDINE
4-BroMo-N-Boc-piperidine
1-N-BOC-4-BROMOPIPERIDINE
1-tert-Butoxycarbonyl-4-bromopiperidine
tert-Butyl 4-bromopiperidine-1-carboxylate
1-Piperidinecarboxylic acid, 4-bromo-, 1,1-dimethylethyl ester | [EINECS(EC#)]
278-340-6 | [Molecular Formula]
C10H18BrNO2 | [MDL Number]
MFCD04115039 | [MOL File]
180695-79-8.mol | [Molecular Weight]
264.16 |
| Chemical Properties | Back Directory | [Melting point ]
42 °C | [Boiling point ]
100-118 °C/0.5 mmHg | [density ]
1.3403 g/mL at 25 °C | [refractive index ]
n20/D 1.4905 | [Fp ]
110 °C | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
powder to lump | [pka]
-2.77±0.40(Predicted) | [color ]
White to Light yellow | [InChI]
InChI=1S/C10H18BrNO2/c1-10(2,3)14-9(13)12-6-4-8(11)5-7-12/h8H,4-7H2,1-3H3 | [InChIKey]
KZBWIYHDNQHMET-UHFFFAOYSA-N | [SMILES]
N1(C(OC(C)(C)C)=O)CCC(Br)CC1 | [CAS DataBase Reference]
180695-79-8 |
| Hazard Information | Back Directory | [Uses]
N-Boc-4-Bromopiperidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| [Synthesis]
Step 1: Synthesis of tert-butyl 4-bromopiperidine-1-carboxylate
To a 35 mL dichloromethane suspension containing 5 g (0.02 mol) of 4-bromopiperidine hydrobromide, 7.09 mL (0.04 mol) of N,N-diisopropylethylamine was added slowly and dropwise at 0 °C. The reaction mixture was stirred for 30 minutes and then continued with the dropwise addition of 6.67 g (0.031 mol) of di-tert-butyl dicarbonate to a 35 mL dichloromethane solution. The reaction mixture was stirred at room temperature for 18 hours. Upon completion of the reaction, the reaction mixture was washed sequentially with 1 M aqueous hydrochloric acid (2 x 30 mL) and brine (30 mL). The organic layer was separated, dried with anhydrous sodium sulfate, filtered and the filtrate was concentrated under reduced pressure to give 6.9 g of 4-bromopiperidine-1-carboxylic acid tert-butyl ester as a yellow oil in quantitative yield. The product was characterized by 1H NMR (250 MHz, chloroform-d): δ 1.46 (9H, s), 1.79-2.00 (2H, m), 2.00-2.16 (2H, m), 3.31 (2H, ddd, J = 13.67,7.73,3.73 Hz), 3.68 (2H, ddd, J = 13.55,6.85,3.65 Hz), 4.34 (1H, tt, J = 7.69,3.81 Hz). | [References]
[1] Patent: US2010/76029, 2010, A1. Location in patent: Page/Page column 42
[2] Patent: US2011/71196, 2011, A1. Location in patent: Page/Page column 22; 23
[3] European Journal of Medicinal Chemistry, 2018, vol. 158, p. 311 - 321
[4] Journal of the American Chemical Society, 2016, vol. 138, # 24, p. 7520 - 7523
[5] Organic Letters, 2000, vol. 2, # 1, p. 6 - 10 |
|
|