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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1739786생성일: 2026년 10월 26일

Hexane → Ammonium Hydroxide

https://huagongshe.com/reaction/1739786

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물(+/-)-trans-1,2,3,4,4a,5,6,7,8,8a-Decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinoneHCID 10517409—
반응물ButyllithiumHCID 178418339—
촉매Benzyltriphenylphosphonium chlorideHCID 70671—
용매TetrahydrofuranHCID 8028—
생성물Ammonium HydroxideHCID 14923—
생성물(+/-)-trans-6-Benzylidene-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)isoquinolineHCID 86754628—

반응 단계

9.9 ml (13.9 mmol) of a 1.4 M solution of n-butyllithium in hexane were added dropwise, under a nitrogen atmosphere and at room temperature, to a suspension of 5.4 g (13.9 mmol) of benzyltriphenylphosphonium chloride in 30 ml of dry THF. The reaction mixture was stirred for 1 h, then a solution of 1 g (3.5 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 was added. The reaction mixture was refluxed 4 h, then cooled and poured onto water and the aqueous phase was extracted with AcOEt. The organic phase was dried over Na2SO4 and the solvent removed in vacuo. The crude reaction mixture was purified by flash chromatography, eluting with a mixture CH2Cl2 /MeOH/conc. NH4OH 90:7:0.7 respectively, yielding 0.94 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05968949
출처 데이터셋uspto-grants-1999_10
ORD IDord-8873cc4ed8fb4a249b44cb7f47806857
출처 메모uspto-grants-1999_10