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Water → 4-Oxazol-5-yl-benzenethiol

HRID 18496
ノート
印刷プレビュー

反応式

HRID 18496 の反応式
[O:1]1[C:5]([C:6]2[CH:11]=[CH:10][C:9]([S:12](Cl)(=O)=O)=[CH:8][CH:7]=2)=[CH:4][N:3]=[CH:2]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O>C1COCC1>[O:1]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]([SH:12])=[CH:10][CH:11]=2)=[CH:4][N:3]=[CH:2]1
参加物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 11776TriphenylphosphineHCID 27764154-(1,3-Oxazol-5-yl)benzenesulphonyl chloride

生成物 1

HCID 685864504-Oxazol-5-yl-benzenethiol収率 89.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 4-oxazol-5-yl-benzenesulfonyl chloride (1 g) in THF (20 ml) was added triphenylphosphine (4.3 g). After stirring at RT for 10 minutes water (2 ml) was added and the reaction was stirred for a further 20 minutes. The reaction was evaporated under reduced pressure and the residue dissolved in EtOAc. The EtOAc solution was extracted with 1M NaOH (×3), the basic extractions were combined, the pH adjusted to 3 using 1M HCl and then re-extracted with EtOAc (×3). The EtOAc fractions were combined and washed with brine, dried (MgSO4) and evaporated under reduced pressure to give the subtitle compound as a green solid (0.65 g).

後処理

  1. additionwas added
  2. customThe reaction was evaporated under reduced pressure
  3. dissolutionthe residue dissolved in EtOAc
  4. extractionThe EtOAc solution was extracted with 1M NaOH (×3)
  5. extractionthe basic extractions
  6. extractionre-extracted with EtOAc (×3)
  7. washwashed with brine
  8. dry with materialdried (MgSO4)
  9. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-21627b31a7604ea3a37ecb8c1bea554f
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07741360B2

反応ノート

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