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Methane, dichloromethoxy- → HCID 19901373, 화합물

HRID 2372664
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HRID 2372664 반응식
[C:1]1([CH3:23])[CH:6]=[CH:5][C:4]([S:7]([O:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:13][CH:12]=2)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[CH3:24][O:25]C(Cl)Cl>ClCCl.[Ti](Cl)(Cl)(Cl)Cl>[C:1]1([CH3:23])[CH:2]=[CH:3][C:4]([S:7]([O:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][C:20]([CH:24]=[O:25])=[CH:19][CH:18]=3)=[CH:13][CH:12]=2)(=[O:8])=[O:9])=[CH:5][CH:6]=1
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참가 물질

5

반응물 2

HCID 21004Methane, dichloromethoxy-HCID 262323Biphenyl-4-yl 4-methylbenzenesulfonate

생성물 1

HCID 19901373HCID 19901373, 화합물

시약·촉매·용매 2

HCID 24193Titanium Tetrachloride촉매HCID 6344Dichloromethane용매

실험 절차

A suspension of 21.06 g of 4-biphenylyl p-toluenesulphonate in 120 ml of dichloromethane was treated at -2° C. while stirring with 23.6 ml of titanium tetrachloride. The mixture was treated dropwise at the same temperature within 30 minutes with 9.63 ml of dichloromethyl methyl ether, stirred at room temperature for a further 1 hour and then poured on to ice. The aqueous phase was separated and extracted with dichloromethane. The combined organic phases were washed with saturated sodium hydrogen carbonate solution and then with water, dried over sodium sulphate and concentrated. Recrystallization of the crude product obtained from 50 ml of ethyl acetate gave 11.65 g of 4'-(p-toluenesulphonyloxy)biphenyl-4-carboxaldehyde.

후처리

  1. additionwas treated at -2° C.
  2. additionpoured on to ice
  3. customThe aqueous phase was separated
  4. extractionextracted with dichloromethane
  5. washThe combined organic phases were washed with saturated sodium hydrogen carbonate solution
  6. dry with materialwith water, dried over sodium sulphate
  7. concentrationconcentrated
  8. customRecrystallization of the crude product
  9. customobtained from 50 ml of ethyl acetate

출처 및 근거

ORD 기록
ord-6e1b929f63f643f49a2cca76443a251f
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05100577

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