1-Acetyl-4-bocamino-piperidine

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1-Acetyl-4-bocamino-piperidine Basic information
Product Name:1-Acetyl-4-bocamino-piperidine
Synonyms:(1-Acetyl-4-piperidinyl)carbamic acid 1,1-dimethylethyl ester;tert-butyl N-(1-acetylpiperidin-4-yl)carbaMate;1-Acetyl-4-Boc-amino-piperidine, 97.5%;tert-butyl 1-acetylpiperidin-4-ylcarbamate;Carbamic acid, N-(1-acetyl-4-piperidinyl)-, 1,1-dimethylethyl ester;tert-butyl N-(1-acetyl-4-piperidyl)carbamate;1-Acetyl-4-bocamino-piperidine
CAS:283167-28-2
MF:C12H22N2O3
MW:242.31
EINECS:
Product Categories:
Mol File:283167-28-2.mol
1-Acetyl-4-bocamino-piperidine Structure
1-Acetyl-4-bocamino-piperidine Chemical Properties
Boiling point 392.9±31.0 °C(Predicted)
density 1.08±0.1 g/cm3(Predicted)
storage temp. 2-8°C
pka12.09±0.20(Predicted)
AppearanceWhite to off-white Solid
Safety Information
Risk Statements 20/21/22
Safety Statements 23-24/25
HS Code 29333990
MSDS Information
1-Acetyl-4-bocamino-piperidine Usage And Synthesis
Synthesis
Acetic anhydride

108-24-7

4-N-BOC-Aminopiperidine

73874-95-0

1-ACETYL-4-BOCAMINO-PIPERIDINE

283167-28-2

4-tert-butoxycarbonylaminopiperidine (5.0 g, 25 mmol) was dissolved in dichloromethane (80 mL) at 0 °C and triethylamine (3.8 g, 38 mmol) and acetic anhydride (2.6 g, 25 mmol) were added sequentially. The reaction mixture was stirred continuously at 0 °C for 2 hours. Upon completion of the reaction, the reaction was quenched by the addition of water (30 mL) and the organic phase was separated and washed with saturated sodium bicarbonate solution (30 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give tert-butyl (1-methylpiperidin-4-yl)carbamate (5.6 g, 93% yield) as a light yellow solid.LC-MS analysis: retention time 1.88 min; mass-to-charge ratio 265.1 [M+Na]+.

References[1] Patent: WO2016/34673, 2016, A1. Location in patent: Page/Page column 91
[2] Patent: WO2016/34675, 2016, A1. Location in patent: Page/Page column 68
[3] Patent: WO2017/153520, 2017, A1. Location in patent: Page/Page column 64
[4] Patent: US2008/227780, 2008, A1. Location in patent: Page/Page column 53-54
[5] Patent: WO2015/198229, 2015, A1. Location in patent: Page/Page column 21
1-Acetyl-4-bocamino-piperidine Preparation Products And Raw materials
Raw materialsAcetic anhydride-->4-N-BOC-Aminopiperidine-->Acetyl chloride-->Dichloromethane-->Triethylamine
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