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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2856생성일: 2026년 10월 23일

Vinyl chloroformate → (+/-)-trans-4a-(3-Methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline hydrochloride

https://huagongshe.com/ko/reaction/2856

반응식

참여 물질

역할이름HCID투입량
반응물Vinyl chloroformateHCID 78808—
반응물Proton spongeHCID 88675—
반응물(+/-)-trans-1,2,3,4,4a,5,6,7,8,8a-Decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinoneHCID 10517409—
용매1,2-DichloroethaneHCID 11—
생성물(+/-)-trans-4a-(3-Methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline hydrochlorideHCID 8675232170.8%

반응 단계

A solution of 1.2 g (4.2 mmol) of (±)-trans-2-ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline and 1.8 g (12.6 mmol) of proton sponge in 34 ml of 1,2-dichloroethane was treated with 1.4 ml (16.8 mmol) of vinylchloroformate at 0° C. under nitrogen atmosphere. The reaction mixture was stirred at this temperature for 15 min and then refluxed for 3 h, the solvent was removed in vacuo, the residue was taken up in water and extracted with Et2O. The organic layer was washed with 3% HCl, then was dried over Na2SO4 and the solvent was removed in vacuo. The dark residue was dissolved in EtOH, 3 ml of concentrated HCl were added and the solution refluxed for 3 hours. The solvent was removed in vacuo, obtaining 0.88 g of the title compound which was used as such in the subsequent step. M.p.=90° C. dec.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731322
출처 데이터셋uspto-grants-1998_03
ORD IDord-65c40f72159b46c38bd188c224445f20
출처 메모uspto-grants-1998_03