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Water → Tetrahydrothiophen-3-yl 4-methylbenzenesulfonate

HRID 256287
ノート
印刷プレビュー

反応式

HRID 256287 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 73974-Toluenesulfonyl chloride2 回HCID 315652Thiolan-3-ol

生成物 1

HCID 13821778Tetrahydrothiophen-3-yl 4-methylbenzenesulfonate収率 50.6%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
16 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-7006f94433194e12989f10dee02a63fa
出典データセット
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04702763

反応ノート

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