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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2189740생성일: 2026년 10월 25일

Hydrochloric Acid → 3-Ethyl-4-(1-piperidinyl)benzoic acid

https://huagongshe.com/reaction/2189740

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물EthanolHCID 702—
반응물Potassium HydroxideHCID 14797—
반응물3-Ethyl-4-(1-piperidinyl)benzonitrileHCID 59316719—
용매WaterHCID 962—
생성물3-Ethyl-4-(1-piperidinyl)benzoic acidHCID 59316788—

반응 단계

3-Ethyl-4-(1-piperidinyl)benzonitrile (D8) (817 mg, 3.82 mmol) and potassium hydroxide (2.14 g, 38.2 mmol) in ethanol (35 mL) and water (8 mL) were heated to 90° C. (block temperature) for 9 h. Further potassium hydroxide (2.14 g, 38.2 mmol) and water (8 mL) were added and the reaction heated for a further 18 h. The reaction was allowed to cool and was neutralised with aqueous HCl. A white solid was separated by filtration and an attempt was made to purify the filtrate by SCX cartridge, but this failed. Both the solid and product of SCX were combined, methanol added and then the mixture acidified with acetic acid. The mixture was filtered to obtain the filtrate, which was then trapped on SCX cartridge, washed with methanol and eluted with 2M ammonia in methanol. On test scale this gave the title compound as a white solid (96 mg, 0.41 mmol) and on the remaining material gave a colourless oil (563 mg, 2.41 mmol). MS (ES): C14H19NO2 requires 233; found 234 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08324254B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-6aad4414bb974d14b72e67d44b8c9bd1
출처 메모uspto-grants-2012_12