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Benzenesulfonyl chloride → HCID 10924734、化合物

HRID 1699479
ノート
印刷プレビュー

反応式

HRID 1699479 の反応式
[SH:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[CH2:9](Br)[C:10]#[CH:11].C(N(CC)CC)C.[C:20]1([S:26](Cl)(=[O:28])=[O:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>C(OCC)(=O)C>[C:20]1([S:26]([O:8][C:5]2[CH:6]=[CH:7][C:2]([S:1][CH2:11][C:10]#[CH:9])=[CH:3][CH:4]=2)(=[O:28])=[O:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 7369Benzenesulfonyl chlorideHCID 7842Propargyl bromideHCID 8471Triethylamine2 回HCID 2401474-Mercaptophenol

生成物 1

HCID 10924734HCID 10924734、化合物収率 109.6%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

4-Mercaptophenol (1) (37.85 g, 300 mmol) and propargyl bromide (42.82 g, 360 mmol) were dissolved in ethyl acetate (757 ml). To the solution was added dropwise triethylamine (42.5 g, 420 mmol) over 25 minutes with stirring and under ice-cooling. After stirring for another 1.5 hours at the same temperature, triethylamine (42.5 g, 420 mmol) was added in one portion, and benzenesulfonyl chloride (63.58 g, 360 mmol) was added dropwise over 20 minutes. After keeping 1 hour at the same temperature, the cooling bath was removed and the mixture was stirred for 30 minutes at room temperature and partitioned into two layers by adding ice-water (500 ml) and 2N hydrochloric acid (110 ml). The aqueous layer was extracted with ethyl acetate (200 ml). The combined organic layer was washed with water, dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to provide 100.04 g of the title compound (2) as oil. Crude yield: 109%.

後処理

  1. temperaturecooling
  2. additionwas added dropwise over 20 minutes
  3. customthe cooling bath was removed
  4. stirringthe mixture was stirred for 30 minutes at room temperature
  5. custompartitioned into two layers
  6. additionby adding ice-water (500 ml) and 2N hydrochloric acid (110 ml)
  7. extractionThe aqueous layer was extracted with ethyl acetate (200 ml)
  8. washThe combined organic layer was washed with water
  9. dry with materialdried over anhydrous magnesium sulfate
  10. distillationthe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-188d2f78bb3544e2ae9af02df83b92e8
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06346628B1

反応ノート

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