돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 231006생성일: 2026년 10월 26일

Hydrochloric Acid → 4'-Methoxy-4-(2-methylbutyryl)biphenyl

https://huagongshe.com/reaction/231006

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-MethoxybiphenylHCID 11943—
반응물Butanoyl chloride, 2-methyl-HCID 93697—
반응물Aluminum(III) ChlorideHCID 6451240—
용매DichloromethaneHCID 6344—
생성물4'-Methoxy-4-(2-methylbutyryl)biphenylHCID 1511394248%

반응 조건

온도0 °C

반응 단계

A solution of 0.15 mole(15.0 g) of (S)-(+)-2-methylbutyric acid and 0.3 mole(35.5 g) of thionyl chloride in 100 ml of chloroform was refluxed for three hours. After chloroform and the excessive thionyl chloride had been distilled out at reduced pressure, the reaction solution was concentrated at reduced pressure to obtain 12.8 g of 2-methylbutyryl chloride. A suspension of 0.1 mole(13.3 g) of aluminium chloride in 100 ml of dry methylene chloride was cooled to 0° C., then 12.8 g of 2-methylbutyryl chloride was added dropwise thereto, and stirred for 30 min. Maintaining the mixed solution at 0° C., a solution of 0.08 mole(14.7 g) of 4-methoxybiphenyl in 80 ml of dry methylene chloride was added dropwise, and stirred for 10 hours at room temperature. The reaction mixture was decomposed by adding into ice and dil. hydrochloric acid, and the organic layer was washed with dil. hydrochloric acid and an aquious sodium hydrogen carbonate solution, and then dried with magnesium sulfate. The concentrated product was purified by column chromatography to obtain 10.3 g of 4'-methoxy-4-(2-methylbutyryl)biphenyl. (yield: 48%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04844835
출처 데이터셋uspto-grants-1989_07
ORD IDord-e29a2677c30e40518e2249eec0c8eb61
출처 메모uspto-grants-1989_07