Carbon tetrabromide → Ethyl 5-(bromomethyl)-1,2-oxazole-3-carboxylate

HRID 58524

反応式

HRID 58524 の反応式
[C:1]([Br:5])(Br)(Br)Br.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.OC[C:27]1[O:31][N:30]=[C:29]([C:32]([O:34][CH2:35][CH3:36])=[O:33])[CH:28]=1>C1COCC1>[Br:5][CH2:1][C:27]1[O:31][N:30]=[C:29]([C:32]([O:34][CH2:35][CH3:36])=[O:33])[CH:28]=1

参加物

5

実験手順

Carbon tetrabromide (5.44 g; 16.39 mmol) was added to the solution of triphenylphosphine (4.34 g, 16.39 mmol) in THF (50 mL) and the resulting mixture was stirred at room temperature for 15 min. To this green suspension was added a solution of ethyl 5-(hydroxymethyl)isoxazole-3-carboxylate (1.87 g, 10.93 mmol) in THF (10 mL) and the resulting reaction mixture was stirred overnight at room temperature. The solid material was removed by filtration. The filtrate was concentrated under reduced pressure and the residue was purified by flash chromatography on silica gel (eluent: 15 to 100% dichloromethane in heptane) to afford 1.73 g (68%) of ethyl 5-(bromomethyl)isoxazole-3-carboxylate as a solid.

後処理

  1. customthe resulting reaction mixture
  2. stirringwas stirred overnight at room temperature
  3. customThe solid material was removed by filtration
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. customthe residue was purified by flash chromatography on silica gel (eluent: 15 to 100% dichloromethane in heptane)

出典と根拠

ORDレコード
ord-3bdb08645a304d71abee182697af6870
出典データセット
uspto-grants-2016_09
特許番号
US09434722B2

関連ノート

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