Benzaldehyde → 5-Phenyl oxazole

HRID 868921ノート

反応式

HRID 868921 の反応式
[CH:1](=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N+:9]([CH2:11]S(C1C=CC(C)=CC=1)(=O)=O)#[C-:10].C([O-])([O-])=O.[K+].[K+]>CO>[C:2]1([C:1]2[O:8][CH:11]=[N:9][CH:10]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 240BenzaldehydeHCID 11430Potassium CarbonateHCID 161915Tosylmethyl isocyanide

生成物 1

HCID 5893115-Phenyl oxazole収率 82.8%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture of benzaldehyde (3 g, 28.3 mmol), 1-(isocyanomethylsulfonyl)-4-methylbenzene (5.5 g, 28.3 mmol) and K2CO3 (5.9 g, 42.5 mmol) in 60 mL methanol was refluxed for 2 h and then concentrated. 250 mL EtOAc was added and the mixture was washed with water and brine, dried, and concentrated to give 5-phenyl oxazole (3.4 g). MS (ESI) m/z 145 (M+H+).

後処理

  1. temperaturewas refluxed for 2 h
  2. concentrationconcentrated
  3. addition250 mL EtOAc was added
  4. washthe mixture was washed with water and brine
  5. customdried
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-b7765c3dcfaa4e14b2a990fe1a6021e7
出典データセット
uspto-grants-2015_03
特許番号
US08969349B2

反応ノート

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