반응 #1543043

ord-0f60be9708fd4d5da0b2bd4e47181571

반응 방정식

CS(=O)(=O)c1ccc(C(=O)Cl)c(Cl)c1
2-chloro-4-methylsulfonylbenzoyl chloride
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
ClC(Cl)C(Cl)Cl
1,1,2,2-tetrachloroethane
Cl
hydrochloric acid
CS(=O)(=O)c1ccc(C(=O)c2c(O)cc(Cl)cc2Cl)c(Cl)c1
2,2', 4'-Trichloro-6'-hydroxy-4-methylsulfonylbenzophenone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the mixture is subsequently refluxed for 7 hours
  2. 2
    기타The organic phase is removed
  3. 3
    추출the aqueous phase is extracted twice
  4. 4
    세척The combined organic phases are washed until neutral and
  5. 5
    추출subsequently extracted three times
  6. 6
    여과The precipitate is filtered off
  7. 7
    세척washed with water until neutral and
  8. 8
    기타dried

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05843869uspto-grants-1998_12