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Water → HCID 11076628, 화합물

HRID 1792313
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HRID 1792313 반응식
[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][CH2:7][OH:8].[C:9]1([CH3:19])[CH:14]=[CH:13][C:12]([S:15](Cl)(=[O:17])=[O:16])=[CH:11][CH:10]=1.O>N1C=CC=CC=1>[C:9]1([CH3:19])[CH:14]=[CH:13][C:12]([S:15]([O:8][CH2:7][CH2:6][O:5][CH2:4][CH2:3][O:2][CH3:1])(=[O:17])=[O:16])=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 73974-Toluenesulfonyl chlorideHCID 8134Diethylene Glycol Monomethyl Ether

생성물 1

HCID 11076628HCID 11076628, 화합물수율 98.4%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of diethylene glycol monomethylether (12 g, 100 mmol) in pyridine (70 ml) was added p-toluenesulfonyl chloride (22.8 g, 120 mmol) at 0° C., which was then stirred at room temperature for 2 hours. Water was added thereto, and the mixture was extracted with diethyl ether. The extracted organic layer was washed with 0.5N-HCl, water and saturated sodium bicarbonate solution, and dried over anhydrous magnesium sulfate. The organic solvent was removed under reduced pressure to give the title compound (27 g, stoichiometric yield) as a yellow oil. The compound thus obtained was used in the next reaction without further purification.

후처리

  1. extractionthe mixture was extracted with diethyl ether
  2. washThe extracted organic layer was washed with 0.5N-HCl, water and saturated sodium bicarbonate solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe organic solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-8c8a90937fc941d6aa4e1f527bfdf07d
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07074819B2

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