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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28263생성일: 2026년 10월 23일

Hydrochloric Acid → (2-Chlorophenyl)(4-chlorophenyl)methanol

https://huagongshe.com/ko/reaction/28263

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-ChlorobenzaldehydeHCID 6996—
반응물p-BromochlorobenzeneHCID 7806—
반응물MagnesiumHCID 5462224—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물(2-Chlorophenyl)(4-chlorophenyl)methanolHCID 247332—

반응 단계

To 12.7 g. (0.52 moles) of magnesium turnings in 200 ml. of anhydrous ether is added 10.0 g. (0.052 moles) of p-bromochlorobenzene, and the mixture is warmed to reflux. When the Grignard reaction begins, the heat is removed and 80.0 g. (0.47 moles) of additional p-bromochlorobenzene in 80 ml. of ether is added dropwise as the refluxing continues. When the addition is completed, the reaction is heated at reflux for 2 hours, cooled, and 73.4 g. (0.52 moles) of o-chlorobenzaldehyde are slowly added. The reaction is refluxed for 2 hours, cooled and poured into iced water. The resulting mixture is made acidic with hydrochloric acid, and the organic phase is separated. The aqueous layer is extracted with ether, and the extract is added to the organic phase. This solution is washed with water, dried over anhydrous magnesium sulfate and concentrated to give an oily solid. The material is crystallized from petroleum ether to give 109.4 g. (83%) of the product, mp 68°-70°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04225723
출처 데이터셋uspto-grants-1980_09
ORD IDord-d1fb74da1fe1496a9557c93116c7aab5
출처 메모uspto-grants-1980_09