Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1004971생성일: 2026년 10월 25일
Potassium Cyanide → tert-butyl (3RS,4RS)-4-(4-cyano-phenyl)-3-hydroxy-piperidine-1-carboxylate
https://huagongshe.com/reaction/1004971
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Cyanide | HCID 9032 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | tert-butyl (3RS,4RS)-4-(4-bromophenyl)-3-hydroxy-piperidine-1-carboxylate | HCID 54537313 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 촉매 | NiBr2(PPh3)2 | HCID 11050914 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | tert-butyl (3RS,4RS)-4-(4-cyano-phenyl)-3-hydroxy-piperidine-1-carboxylate | HCID 54237291 | 56% |
반응 단계
A suspension of 20 mg (0.30 mmol) of activated zinc powder, 76 mg (1.17 mmol) of potassium cyanide, 52 mg (0.20 mmol) of triphenylphosphine and 74 mg (0.10 mmol) of bis(triphenylphosphine)-nickel(II) dibromide in 2 ml of acetonitrile was heated at 60° C. under argon for 5 minutes. 356 mg (1.00 mmol) of tert-butyl (3RS,4RS)-4-(4-bromophenyl)-3-hydroxy-piperidine-1-carboxylate in solid form were added thereto. The green suspension was stirred at 60° C. under argon for 20 hours. The resulting dark brown suspension was filtered over Speedex and the insoluble material was washed with methylene chloride. The filtrate was partitioned between methylene chloride and 5% sodium hydrogen carbonate solution, the organic phase was dried over magnesium sulphate and finally the solvent was removed under reduced pressure. The crude product (416 mg) was purified by chromatography on silica gel with a 1:1 mixture of ethyl acetate and hexane as the eluent. There were obtained 168 mg (56% of theory) of tert-butyl (3RS,4RS)-4-(4-cyano-phenyl)-3-hydroxy-piperidine-1-carboxylate as a colourless solid; MS: 302 (M)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06051712 |
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| 출처 데이터셋 | uspto-grants-2000_04 |
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| ORD ID | ord-dfcd92635c5d4207a60d24ad221b36c5 |
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| 출처 메모 | uspto-grants-2000_04 |
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