참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Methyl 4-(cyanomethyl)benzoate | HCID 848548 | — |
| 반응물 | 3-Bromophenethyl bromide | HCID 14361216 | — |
| 반응물 | HCID 178418922 | HCID 178418922 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Methyl 4-[3-(3-bromophenyl)-1-cyanopropyl]benzoate | HCID 66939300 | 55% |
반응 단계
To a mixed solution of methyl 4-(cyanomethyl)benzoate (3.50 g, 20.0 mmol), tetrahydrofuran (25 mL) and N,N-dimethylformamide (10 ml) was added tert-butoxy potassium (2.69 g, 24.0 mmol) at −78° C., and the mixture was stirred for 30 min. To the reaction mixture was added 1-bromo-3-(2-bromoethyl)benzene (3.37 mL, 22.0 mmol) at the same temperature, and the mixture was stirred under ice-cooling for 4 hr. The reaction mixture was diluted with water, extracted with ethyl acetate, washed successively with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate) to give the title compound (3.94 g, 55%) as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08461348B2 |
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| 출처 데이터셋 | uspto-grants-2013_06 |
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| ORD ID | ord-42dd959c09e7445aa431ff3d0d1e2b41 |
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| 출처 메모 | uspto-grants-2013_06 |
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