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1,3-Dichloroacetone → 4-[2-(4-Chloromethyl-2-oxazolyl)ethyl]-5-methyl-2-phenyloxazole

HRID 1294180
ノート
印刷プレビュー

反応式

HRID 1294180 の反応式
[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:13][CH2:14][C:15]([NH2:17])=[O:16].[Cl:18][CH2:19][C:20](=O)[CH2:21]Cl.C(=O)([O-])[O-].[K+].[K+]>>[Cl:18][CH2:19][C:20]1[N:17]=[C:15]([CH2:14][CH2:13][C:3]2[N:4]=[C:5]([C:7]3[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=3)[O:6][C:2]=2[CH3:1])[O:16][CH:21]=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 3

HCID 107931,3-DichloroacetoneHCID 11430Potassium CarbonateHCID 178613843-(5-Methyl-2-phenyl-4-oxazolyl)propanamide

生成物 1

HCID 178612164-[2-(4-Chloromethyl-2-oxazolyl)ethyl]-5-methyl-2-phenyloxazole収率 18%

反応条件

温度
130 °C

実験手順

A mixture of 3-(5-methyl-2-phenyl-4-oxazolyl)propanamide (10.0 g) and 1,3-dichloro-2-propanone (5.35 g) was stirred at 130° C. for 2 hrs. An aqueous potassium carbonate solution was added to alkalize the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The residue was subjected to silica gel column chromatography to give crystals (2.30 g, 18%) of 4-[2-(4-chloromethyl-2-oxazolyl)ethyl]-5-methyl-2-phenyloxazole from a fraction eluted with ethyl acetate-hexane (1:4, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 71-72° C.

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate

出典と根拠

ORDレコード
ord-3ba4c36890a8468588265f4c9e0c02b6
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07238716B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート