반응 #1543043
ord-0f60be9708fd4d5da0b2bd4e47181571
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후처리
- 1온도the mixture is subsequently refluxed for 7 hours
- 2기타The organic phase is removed
- 3추출the aqueous phase is extracted twice
- 4세척The combined organic phases are washed until neutral and
- 5추출subsequently extracted three times
- 6여과The precipitate is filtered off
- 7세척washed with water until neutral and
- 8기타dried
실험 절차
3.00 g of 2-chloro-4-methylsulfonylbenzoyl chloride are added in portions at room temperature to a mixture of 1.97 g of 3,5-dichlorophenone and 3.23 g of aluminum chloride in 50 ml of 1,1,2,2-tetrachloroethane, and the mixture is subsequently refluxed for 7 hours. When cold, the reaction mixture is poured onto 100 g of ice and 20 ml of concentrated hydrochloric acid. The organic phase is removed, and the aqueous phase is extracted twice using 50 ml of dichloromethane. The combined organic phases are washed until neutral and subsequently extracted three times using in each case 25 ml of 2N sodium hydroxide solution. The combined alkaline extracts are brought to a pH of 2 using concentrated hydrochloric acid. The precipitate is filtered off, washed with water until neutral and dried. This gives 3.194 g (70% of theory) of 2,2', 4'-trichloro-6'-hydroxy-4-methylsulfonylbenzophenone in the form of colorless crystals with a melting point of 123°-126° C.