Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26479생성일: 2026년 10월 26일
Phenethyl bromide → N-Phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline
https://huagongshe.com/reaction/26479
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Phenethyl bromide | HCID 7666 | — |
| 반응물 | Pentane | HCID 8003 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4a-(m-Methoxyphenyl)-1,3-diketo-trans-decahydroisoquinoline | HCID 86736478 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-Phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline | HCID 13282015 | — |
반응 단계
A solution of 10.0 g (37 mmoles) of 4a-(m-methoxyphenyl)-1,3-diketo-trans-decahydroisoquinoline in 250 ml of anhydrous dimethylformamide was added with stirring to a suspension of 2.8 g (55.5 mmoles) of 50% sodium hydride in mineral oil (washed with pentane) in 125 ml of anhydrous dimethylformamide heated at 50° under nitrogen. The mixture was heated at 90° for 2 hours, then cooled to 40°, at which time a solution of 14.0 g (74 mmoles) of phenethyl bromide in 20 ml of anhydrous dimethylformamide was added and the reaction mixture heated at 90° overnight. The cooled solution was poured into ice-water and extracted with ether. Evaporation of the ether gave an oil which was purified by column chromatography (Silicar CC-7, eluting with acetone-benzene). The major fraction was identified as N-phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04150135 |
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| 출처 데이터셋 | uspto-grants-1979_04 |
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| ORD ID | ord-39d377ee3df3459fbf811c3daf211de4 |
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| 출처 메모 | uspto-grants-1979_04 |
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