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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1533165생성일: 2026년 10월 25일

Chloroacetyl chloride → 1-(4-Benzylpiperidin-1-yl)-2-chloroethan-1-one

https://huagongshe.com/reaction/1533165

반응식

참여 물질

역할이름HCID투입량
반응물Chloroacetyl chlorideHCID 6577—
반응물Potassium CarbonateHCID 11430—
반응물4-BenzylpiperidineHCID 31738—
용매TetrahydrofuranHCID 8028—
생성물1-(4-Benzylpiperidin-1-yl)-2-chloroethan-1-oneHCID 112960891.5%

반응 단계

A solution of 4-benzylpiperidine (17.5 g, 100 mmol) in THF (250 mL) was treated with K2CO3 (14 g, 101 mmol) and chloroacetylchloride (11.3 g, 100 mmol) at rt for 2 hours. The reaction mixture was filtered. The filtrate was concentrated, and then dissolved in EtOAc and water. The 25 organic layer was washed with brine, dried over MgSO4, and concentrated to give the product (21.6 g, 91.5%). 1H NMR (CDCl3) δ 7.32-7.12 (m, 5H), 4.09 (s, 2H), 3.79-3.76 (m, 2H), 2,56 (d, J=7.0 Hz, 2H), 1.89-1.80 (m, 1H), 1.79-1.71 (m, 4H), 1.28-1.12 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06207697B1
출처 데이터셋uspto-grants-2001_03
ORD IDord-206f674c37f54c77b69fd9574e83212e
출처 메모uspto-grants-2001_03