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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375489생성일: 2026년 10월 24일

Triethylamine → HCID 67745322, 화합물

https://huagongshe.com/ko/reaction/375489

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-(2-(Dimethylamino)phenyl)acetic acidHCID 20466109—
반응물(4aRS,7aRS)4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole hydrochlorideHCID 67745331—
용매DichloromethaneHCID 6344—
생성물HCID 67745322HCID 6774532278.5%

반응 단계

1.18 g of N,N'-carbonyldiimidazole are added to a solution of 1.16 g of 2-dimethylaminophenylacetic acid in 20 cm3 of dry dichloromethane. The mixture is stirred for 30 minutes at +5° C. and then a solution of 2.0 g of (4aRS,7aRS)-4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole hydrochloride and 1.83 cm3 of triethylamine in 20 cm3 of dichloromethane is added. The reaction mixture is stirred for 1 hour at 20° C. and is then washed twice with 50 cm3 of water and dried over magnesium sulphate. The solution is filtered and concentrated to dryness under reduced pressure (2.7 kPa). The oil obtained is chromatographed on a silica gel column (0.04 mm-0.06 mm, diameter 2.8 cm, height 26 cm), eluting under a nitrogen pressure of 0.6 bar with a cyclohexane and ethyl acetate mixture of (60/40 by volume) and collecting fractions of 60 cm 3 . Fractions 6 to 20 are pooled and concentrated to dryness under reduced pressure (2.7 kPa) and the residue is crystallized from an acetonitrile and diisopropyl oxide mixture. The crystals are drained and dried. 2.16 g of (4aRS,7aRS)-6-[(2-dimethylaminophenyl)acetyl]-4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole are obtained in the form of a white solid; melting point 163° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05484942
출처 데이터셋uspto-grants-1996_01
ORD IDord-4dd01b6958d049949ec91cc243ca44b2
출처 메모uspto-grants-1996_01