참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 1-(p-Tolyl)piperazine dihydrochloride | HCID 83112 | — |
| 반응물 | 3-Bromo-2,2-dimethylpropanoic acid | HCID 271932 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-Bromo-1-(4-methylphenyl)piperazine 2,2-dimethylpropan-1-one | HCID 86635778 | 52% |
반응 단계
3-Bromo-2,2-dimethylpropionic acid (10.0 g, 55.3 mmol) was dissolved in DCM (60 mL). Oxalyl chloride (7.20 mL, 82.9 mmol) was added slowly over 10 minutes. The reaction mixture was stirred at room temperature for 18 hours and then concentrated in vacuo. The residue was dissolved in DCM (40 mL) and added to a solution of 4-methylphenyl-piperazine dihydrochloride (13.76 g, 55.3 mmol) and DIPEA (33.0 mL, 193.4 mmol) in DCM (100 mL) at 0° C. The reaction mixture was allowed to warm to room temperature over 1 hour and then stirred at room temperature for 16 hours. The reaction mixture was washed with 10% citric acid solution (2×100 mL), dried (MgSO4) and concentrated in vacuo to give 3-bromo-1-(4-methylphenyl)piperazine-2,2-dimethylpropan-1-one (9.62 g, 52%) as a white solid which was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08093248B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-43dd9f090fc14470b0593744eb01787f |
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| 출처 메모 | uspto-grants-2012_01 |
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