N-BOC-(2S)-PYRR(2-CHCN)

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Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:(s)-tert-butyl 2-(cyanomethyl)pyrrolidine-1-carboxylate
CAS:142253-50-7
Purity:0.99 Package:1kg
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Products Intro: Product Name:N-BOC-(2S)-PYRR(2-CHCN)
CAS:142253-50-7
Purity:99.0% Package:1g;1USD
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Products Intro: Product Name: N-BOC-(2S)-PYRR(2-CHCN)
CAS:142253-50-7
Purity:Min98% HPLC/GC Package:1g;8.88USD
Company Name: Blocksynth Pharmaceutical Technology Co.,Ltd
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Products Intro: Product Name:(S)-TERT-BUTYL 2-(CYANOMETHYL)PYRROLIDINE-1-CARBOXYLATE
CAS:142253-50-7
Purity:98% Package:25KG;USD
Company Name: Suzhou ARTK Medchem Co., Ltd.
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Products Intro: Product Name:tert-butyl(2S)-2-(cyanomethyl)pyrrolidine-1-carboxylate
CAS:142253-50-7
Purity:0.98 Package:100KG;25KG;10KG;1KG

N-BOC-(2S)-PYRR(2-CHCN) manufacturers

N-BOC-(2S)-PYRR(2-CHCN) Basic information
Product Name:N-BOC-(2S)-PYRR(2-CHCN)
Synonyms:1-Pyrrolidinecarboxylic acid, 2-(cyanoMethyl)-, 1,1-diMethylethyl ester, (2S)-;(S)-1-Boc-2-(cyanomethyl)pyrrolidine;N-BOC-(2S)-PYRR(2-CHCN);(S)-TERT-BUTYL 2-(CYANOMETHYL)PYRROLIDINE-1-CARBOXYLATE;tert-butyl (2S)-2-(cyanomethyl)pyrrolidine-1-carboxylate;2-(cyanomethyl)-1-pyrrolidinecarboxylic acid tert-butyl ester;(S)-N-Boc-pyrrolidylacetonitrile;(S)-1-Boc-2-(cyanomethyl)pyrrolidine - [C14132]
CAS:142253-50-7
MF:C11H18N2O2
MW:210.27
EINECS:
Product Categories:
Mol File:142253-50-7.mol
N-BOC-(2S)-PYRR(2-CHCN) Structure
N-BOC-(2S)-PYRR(2-CHCN) Chemical Properties
Boiling point 327.4±15.0 °C(Predicted)
density 1.062±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka-2.57±0.40(Predicted)
AppearanceLight yellow to brown Liquid
Safety Information
MSDS Information
N-BOC-(2S)-PYRR(2-CHCN) Usage And Synthesis
Synthesis
sodium:cyanide

773837-37-9

(S)-TERT-BUTYL 2-(TOSYLOXYMETHYL)PYRROLIDINE-1-CARBOXYLATE

86661-32-7

N-BOC-(2S)-PYRR(2-CHCN)

142253-50-7

The general procedure for the synthesis of tert-butyl (S)-2-(cyanomethyl)pyrrolidine-1-carboxylate from the compound (CAS: 773837-37-9) and tert-butyl (S)-2-((tolylenesulfonyloxy)methyl)pyrrolidine-1-carboxylate was as follows: to a solution of dimethyl sulfoxide (255 mL) of intermediate 6 (90.4 g, 255 mmol) was added sodium cyanide ( 16.2 g, 331 mmol) and the mixture was heated to 100 °C. The reaction mixture was stirred at 100 °C for 4 h. After cooling to room temperature, the mixture was diluted with the addition of water. The aqueous layer was extracted with ethyl acetate and the organic layers were combined. The organic layer was washed sequentially with water and saturated brine and then dried over anhydrous sodium sulfate. The dried organic phase was concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography with the eluent of petroleum ether/ethyl acetate (70/30 to 30/70, v/v) to afford tert-butyl (S)-2-(cyanomethyl)pyrrolidine-1-carboxylate (35.2 g, 168 mmol, 66% yield). Mass spectrometry (ESI+) showed the molecular ion peak m/z 211 ([M+H]+, 100%).

References[1] Patent: WO2011/111875, 2011, A1. Location in patent: Page/Page column 63-64
[2] Patent: WO2012/154676, 2012, A1. Location in patent: Page/Page column 180
[3] Patent: WO2014/71368, 2014, A1. Location in patent: Paragraph 00410
[4] Patent: WO2016/196393, 2016, A2. Location in patent: Paragraph 00277
N-BOC-(2S)-PYRR(2-CHCN) Preparation Products And Raw materials
Raw materialsPOTASSIUM CYANIDE-->sodium:cyanide-->(S)-TERT-BUTYL 2-(TOSYLOXYMETHYL)PYRROLIDINE-1-CARBOXYLATE
Tag:N-BOC-(2S)-PYRR(2-CHCN)(142253-50-7) Related Product Information
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