4-Toluenesulfonyl chloride → HCID 18411913, 화합물

HRID 896526노트

반응식

HRID 896526 반응식
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][OH:11])=[CH:5][CH:4]=1.[C:14]1([CH3:24])[CH:19]=[CH:18][C:17]([S:20](Cl)(=[O:22])=[O:21])=[CH:16][CH:15]=1>N1C=CC=CC=1>[F:1][C:2]([F:12])([F:13])[C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH2:10][O:11][S:20]([C:17]2[CH:18]=[CH:19][C:14]([CH3:24])=[CH:15][CH:16]=2)(=[O:22])=[O:21])=[CH:7][CH:8]=1

참가 물질

4

반응물 2

HCID 73974-Toluenesulfonyl chlorideHCID 112755102-(4-(Trifluoromethyl)phenyl)ethan-1-ol

생성물 1

HCID 18411913HCID 18411913, 화합물수율 80%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 2-(4-trifluoromethylphenyl)-ethanol (570 mg, 3.0 mmol) in pyridine (6 mL) was stirred on an ice/acetone bath and treated with p-toluenesulfonyl chloride (630 mg, 3.3 mmol). The cooling bath was replaced with an ice/water bath and the mixture was stirred for 3.5 hours. Ice-cold water (12 mL) was added slowly, and the mixture was extracted three times with chloroform. The combined organic phases were washed with water, then with cold 1.0 N aqueous sulfuric acid until the wash phase was acidic. The organic phase was dried over sodium sulfate and concentrated to provide a white solid (826 mg) which contained about 10% by weight of residual alcohol. This was used without further purification. 1H NMR (300 MHz, CDCl3) for toluenesulfonate: δ7.65 (d, J=8 Hz, 2H), 7.50 (d, J=8 Hz, 2H), 7.26 (d, J=8 Hz, 2H), 7.23 (d, J=8 Hz, 2H), 4.26 (t, J=7 Hz, 2H), 3.02 (t, J=7 Hz, 2H), 2.44 (s, 3H).

후처리

  1. customThe cooling bath was replaced with an ice/water bath
  2. extractionthe mixture was extracted three times with chloroform
  3. washThe combined organic phases were washed with water
  4. dry with materialThe organic phase was dried over sodium sulfate
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ade26f5432b84c6bb841dbadd5e0ba2d
출처 데이터셋
uspto-grants-2005_07
특허 번호
US06919356B2

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