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HRID 28263作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2-ChlorobenzaldehydeHCID 6996—
反応物p-BromochlorobenzeneHCID 7806—
反応物MagnesiumHCID 5462224—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物(2-Chlorophenyl)(4-chlorophenyl)methanolHCID 247332—

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04225723
出典データセットuspto-grants-1980_09
ORD IDord-d1fb74da1fe1496a9557c93116c7aab5
出典メモuspto-grants-1980_09