تفاعل #1543043

ord-0f60be9708fd4d5da0b2bd4e47181571

معادلة التفاعل

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

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture is subsequently refluxed for 7 hours
  2. 2
    أخرىThe organic phase is removed
  3. 3
    استخلاصthe aqueous phase is extracted twice
  4. 4
    غسيلThe combined organic phases are washed until neutral and
  5. 5
    استخلاصsubsequently extracted three times
  6. 6
    ترشيحThe precipitate is filtered off
  7. 7
    غسيلwashed with water until neutral and
  8. 8
    أخرىdried

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05843869uspto-grants-1998_12