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HRID 1739786作成日:2026年10月27日

Hexane → Ammonium Hydroxide

https://huagongshe.com/reaction/1739786

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物(+/-)-trans-1,2,3,4,4a,5,6,7,8,8a-Decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinoneHCID 10517409—
反応物ButyllithiumHCID 178418339—
触媒Benzyltriphenylphosphonium chlorideHCID 70671—
溶媒TetrahydrofuranHCID 8028—
生成物Ammonium HydroxideHCID 14923—
生成物(+/-)-trans-6-Benzylidene-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)isoquinolineHCID 86754628—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05968949
出典データセットuspto-grants-1999_10
ORD IDord-8873cc4ed8fb4a249b44cb7f47806857
出典メモuspto-grants-1999_10