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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1739781생성일: 2026년 10월 27일

1,3-Dibromobenzene → (+/-)-trans-6-(3-Bromophenyl)-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinol

https://huagongshe.com/reaction/1739781

반응식

참여 물질

역할이름HCID투입량
반응물1,3-DibromobenzeneHCID 7927—
반응물(+/-)-trans-1,2,3,4,4a,5,6,7,8,8a-Decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinoneHCID 10517409—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Ammonium HydroxideHCID 14923—
생성물(+/-)-trans-6-(3-Bromophenyl)-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinolHCID 8675462347.5%

반응 단계

8.9 ml (12.5 mmol) of a 1.4 M solution of n-butyllithium in hexane were added dropwise, under a nitrogen atmosphere and at -55° C., to a solution of 2.95 g (12.5 mmol) of 1,3-dibromobenzene in 10 ml of dry THF. After 90 min this solution was added via cannula to a solution of 1.2 g (4.17 mmol) of (±)-trans-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinone in 10 ml of dry THF and at -20° C. The reaction mixture was allowed to warm up to room temperature overnight, then it was quenched with a saturated NH4Cl solution. The aqueous phase was extracted with AcOEt and the solvent was removed in vacuo. The residue was taken up in Et2O and washed with a 10% HCl solution; the phases were separated and the aqueous phase was brought to pH 14 with a 2N NaOH solution, then extracted with CH2Cl2. The organic phase was dried over Na2SO4, the solvent was removed in vacuo and the crude reaction mixture was purified by flash chromatography, eluting with a mixture CH2Cl2 /MeOH/conc. NH4OH 94.5:5:0.5 respectively, yielding 0.44 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05968949
출처 데이터셋uspto-grants-1999_10
ORD IDord-80b29c1eea714875a3ea9661f6672ec4
출처 메모uspto-grants-1999_10