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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 581847생성일: 2026년 10월 26일

Oxalyl chloride → HCID 11727386, 화합물

https://huagongshe.com/reaction/581847

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물(17beta)-3-Oxoandrost-4-ene-17-carboxylic acidHCID 99472—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물HCID 11727386HCID 11727386—

반응 조건

온도0 °C

반응 단계

To a stirred solution of 3-oxoandrost-4-ene-17β-carboxylic acid (30 g) in methylene chloride (300 mL) and dimethylformamide (1.82 mL) a solution of oxalyl chloride (9.28 mL) in methylene chloride (30 mL) was added dropwise at 0° C. under nitrogen atmosphere. After stirring at 0° C. for 1 hour the reaction was completed. The volatile compounds were removed under vacuum, the solid was taken up with cyclohexane (200 mL) and evaporated to dryness (twice). The 3-oxo-androst-4-ene-17β-carbonyl chloride (30.33 g) so obtained was dissolved in chloroform (1.5 L), cooled to 0° C. and treated with 1,1,1,3,3,3-hexafluorophenylpropyl amine (46.078 g) and pyridine (38.3 mL). The reaction mixture was heated at reflux for 7 hours. After staying overnight at room temperature the reaction mixture was washed with 1N HCl (2×100 mL), with brine, with water until neutral and dried over sodium sulfate. The solvent was evaporated under vacuum and the brownish solid purified by flash chromatography on silica gel (eluant: n-hexane/ethyl acetate 70/30) to yield 9.2 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05922728
출처 데이터셋uspto-grants-1999_07
ORD IDord-c62ab4dc7f4b4dc981a99e191ac969c0
출처 메모uspto-grants-1999_07