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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417990생성일: 2026년 10월 25일

Oxalyl chloride → 3-Bromo-1-(4-methylphenyl)piperazine 2,2-dimethylpropan-1-one

https://huagongshe.com/reaction/417990

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물1-(p-Tolyl)piperazine dihydrochlorideHCID 83112—
반응물3-Bromo-2,2-dimethylpropanoic acidHCID 271932—
용매DichloromethaneHCID 6344—
생성물3-Bromo-1-(4-methylphenyl)piperazine 2,2-dimethylpropan-1-oneHCID 8663577852%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093248B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-43dd9f090fc14470b0593744eb01787f
출처 메모uspto-grants-2012_01