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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432789생성일: 2026년 10월 26일

Benzoyl chloride → Ethyl 1-benzoyl-3-piperidinecarboxylate

https://huagongshe.com/reaction/432789

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물DiisopropylethylamineHCID 81531—
반응물Ethyl nipecotateHCID 98969—
용매DichloromethaneHCID 6344—
생성물Ethyl 1-benzoyl-3-piperidinecarboxylateHCID 378439495.6%

반응 단계

Commercially available ethyl nipecotate (1.48 ml; 9.53 mmol) was dissolved in dichloromethane (20 ml), and diisopropylethylamine (1.82 ml; 10.45 mmol) was added. Benzoyl chloride (1.1 ml; 9.53 mmol) was then added slowly to control any rise in reaction temperature. After addition was complete the mixture was allowed to stir at ambient temperature for approximately 1-4 hours. The mixture was then diluted with fresh dichloromethane and washed with 1 N HCl. The dichloromethane solution was dried with anhydrous potassium carbonate and evaporated at ambient temperature under reduced pressure. The crude material was purified by high-vacuum distillation at approximately 200° C./0.1 torr giving ethyl 1-benzoyl-3-piperidinecarboxylate (2.38 g) as a colorless oil. (The temperatures given for distillations in these examples are oven temperatures and represent approximations. Similarly, the vacuum levels given for distillations are also approximates.) MS m/z (positive ion) 545 (dimer+; 25), 284 (M+Na+; 90), 262 (MH+; 100), 216 (25).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06664271B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-aa11302365da476296f1ec8e31b39aa9
출처 메모uspto-grants-2003_12