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Borane;tetrahydrofuran → 4-(5-Oxazolyl)benzylamine

HRID 1186896
ノート
印刷プレビュー

反応式

HRID 1186896 の反応式
[O:1]1[C:5]([C:6]2[CH:14]=[CH:13][C:9]([C:10]([NH2:12])=O)=[CH:8][CH:7]=2)=[CH:4][N:3]=[CH:2]1.B.C1COCC1>C1COCC1>[O:1]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]([CH2:10][NH2:12])=[CH:13][CH:14]=2)=[CH:4][N:3]=[CH:2]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

4

反応物 2

HCID 2723981Borane;tetrahydrofuranHCID 219309994-(5-Oxazolyl)-benzamide

生成物 1

HCID 219309934-(5-Oxazolyl)benzylamine収率 32.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

A suspension of 4-(5-oxazolyl)benzamide (500 mg, 2.657 mmol) in 10 mL of dry THF was cooled to 0° C. and 10 mL of 1M BH3.THF (10.00 mmol) was added. The contents were refluxed overnight and the excess borane was destroyed by dropwise addition of methanol. The solvent was evaporated and the residue was treated with methanolic HCl to decompose the amine-borane complex. After evaporation of the methanol, the residue was taken in water, basified to pH 10 and the product was extracted in to DCM. The DCM layer was dried (K2CO3) and the solvent was removed to provide 150 mg (32%) of 4-(5-oxazolyl)benzylamine: 1H NMR (CDCl3) δ 7.90 (s, 1H), 7.60 (d, 2H), 7.40 (d, 2H), 7.30 (s, 1H), 3.90 (s, 2H).

後処理

  1. temperatureThe contents were refluxed overnight
  2. customthe excess borane was destroyed by dropwise addition of methanol
  3. customThe solvent was evaporated
  4. additionthe residue was treated with methanolic HCl
  5. customAfter evaporation of the methanol
  6. extractionthe product was extracted in to DCM
  7. dry with materialThe DCM layer was dried (K2CO3)
  8. customthe solvent was removed

出典と根拠

ORDレコード
ord-7545fb8832b6405c8f546a1283b19197
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08673924B2

反応ノート

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