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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 262206생성일: 2026년 10월 27일

Hydrochloric Acid → 4-(4-Methoxybenzyl)cyclohexanecarboxylic acid

https://huagongshe.com/reaction/262206

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1-Cyclohexene-1-carboxylic acidHCID 69470—
반응물4-(4-Methoxybenzyl)benzoic acidHCID 257987—
반응물SodiumHCID 5360545—
용매Isoamyl AlcoholHCID 31260—
생성물4-(4-Methoxybenzyl)cyclohexanecarboxylic acidHCID 12463844—

반응 단계

A solution of 49.5 g. of 4-(4-methoxybenzyl)benzoic acid (Example 1c) in 1000 ml. of isoamyl alcohol was heated at reflux and 109 g. of sodium was added in pieces over a 40 minute period. The reaction mixture was heated under reflux for three hours, then cooled and steam distilled until 2.5 liters of distillate was obtained. The resulting aqueous solution was acidified with concentrated hydrochloric acid and extracted with ether. The ether extracts were dried over anhydrous magnesium sulfate and the solvent removed to give 34 g. of a crystalline residue comprising a mixture of the desired compound with the corresponding cyclohex-1-enecarboxylic acid. The latter mixture was dissolved in 170 ml. of ethanol and hydrogenated in the presence of 3 g. of 10% palladium-on-carbon catalyst. The catalyst was filtered off and the solvent removed to give 34 g. of 4-(4-methoxybenzyl)cyclohexanecarboxylic acid, used directly in the next reaction without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04153719
출처 데이터셋uspto-grants-1979_05
ORD IDord-d825497ddc644ca18bbbb67c5831e7d9
출처 메모uspto-grants-1979_05