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Water → Tetrahydrothiophen-3-yl 4-methylbenzenesulfonate

HRID 256287
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인쇄 미리보기

반응식

HRID 256287 반응식
[S:1]1[CH2:5][CH2:4][CH:3]([OH:6])[CH2:2]1.[CH3:7][C:8]1[CH:13]=[CH:12][C:11]([S:14](Cl)(=[O:16])=[O:15])=[CH:10][CH:9]=1.O>N1C=CC=CC=1>[CH3:7][C:8]1[CH:13]=[CH:12][C:11]([S:14]([O:6][CH:3]2[CH2:4][CH2:5][S:1][CH2:2]2)(=[O:16])=[O:15])=[CH:10][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 73974-Toluenesulfonyl chloride2회HCID 315652Thiolan-3-ol

생성물 1

HCID 13821778Tetrahydrothiophen-3-yl 4-methylbenzenesulfonate수율 50.6%

시약·촉매·용매 1

HCID 1049Pyridine용매

반응 조건

온도
16 °C

실험 절차

To a chilled solution of 1.12 g (0.0098 mole) of tetrahydrothiophene-3-ol in 15 mL of pyridine was added 1.91 g (0.01 mole) of 4-methylphenylsulfonyl chloride, and the reaction mixture was stirred in the cold, about 16° C., for 1 hour then placed in a cold refrigerator for 16 hours. The reaction mixture was allowed to warm to room temperature and was stirred for 1 hour. An additional 0.3 g (0.0016 mole) of 4-methylphenylsulfonyl chloride was added, and the reaction mixture was stirred at room temperature for 64 hours. The reaction mixture was poured into water, and the whole was extracted with methylene chloride. The methylene chloride solution was dried and concentrated to give 1.28 g of product as an oil.

후처리

  1. temperatureto warm to room temperature
  2. stirringwas stirred for 1 hour
  3. stirringthe reaction mixture was stirred at room temperature for 64 hours
  4. extractionthe whole was extracted with methylene chloride
  5. dry with materialThe methylene chloride solution was dried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-7006f94433194e12989f10dee02a63fa
출처 데이터셋
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04702763

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