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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40751생성일: 2026년 10월 23일

Trimethylsilyldiazomethane → Methyl 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylate

https://huagongshe.com/ko/reaction/40751

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물1-(3-Bromo-5-cyanophenyl)piperidine-4-carboxylic acidHCID 59588189—
용매MethanolHCID 887—
용매TolueneHCID 1140—
생성물Methyl 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylateHCID 59588037100%

반응 단계

To a solution of 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylic acid (1.1 g, 3.6 mmol) in toluene (4 mL) and methanol (2 mL) was added TMSCHN2 (2 M in Et2O, 3.5 mL, 7.0 mmol) dropwise at room temperature. After 1 h, the reaction was quenched with acetic acid (˜0.1 mL), diluted with EtOAc and washed with saturated aqueous NaHCO3. The organic layer was separated, dried (MgSO4), and concentrated to give methyl 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylate in ˜100% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530480B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-852a98529a0f4ee78c517dafdbe85afc
출처 메모uspto-grants-2013_09