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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

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참여 물질

역할이름HCID투입량
반응물Potassium CyanideHCID 9032—
반응물TriphenylphosphineHCID 11776—
반응물tert-butyl (3RS,4RS)-4-(4-bromophenyl)-3-hydroxy-piperidine-1-carboxylateHCID 54537313—
촉매ZincHCID 23994—
촉매NiBr2(PPh3)2HCID 11050914—
용매AcetonitrileHCID 6342—
생성물tert-butyl (3RS,4RS)-4-(4-cyano-phenyl)-3-hydroxy-piperidine-1-carboxylateHCID 5423729156%

반응 조건

온도60 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06051712
출처 데이터셋uspto-grants-2000_04
ORD IDord-dfcd92635c5d4207a60d24ad221b36c5
출처 메모uspto-grants-2000_04