Potassium Carbonate → 3-Phenoxybenzyl 2-(2benzothienyl)-3-methylbutanoate

HRID 27925

反応式

HRID 27925 の反応式
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[CH:3]=[C:2]1[CH:10]([CH:14]([CH3:16])[CH3:15])[C:11]([OH:13])=[O:12].[O:17]([C:24]1[CH:25]=[C:26]([CH:29]=[CH:30][CH:31]=1)[CH2:27]Br)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.C([O-])([O-])=O.[K+].[K+]>C1COCC1.CN(P(N(C)C)(N(C)C)=O)C.CCOCC>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[CH:3]=[C:2]1[CH:10]([CH:14]([CH3:16])[CH3:15])[C:11]([O:13][CH2:27][C:26]1[CH:29]=[CH:30][CH:31]=[C:24]([O:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:25]=1)=[O:12]

参加物

6

反応物 3

HCID 11430Potassium CarbonateHCID 945441-(Bromomethyl)-3-phenoxybenzeneHCID 233403922-(1-Benzothiophen-2-yl)-3-methylbutanoic acid

生成物 1

HCID 131463503-Phenoxybenzyl 2-(2benzothienyl)-3-methylbutanoate

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 86583969tetrahydrofuran HMPA溶媒

実験手順

A mixture of 2-(2-benzothienyl)-3-methylbutanoic acid (1 g, 4.3 mmol), 3-phenoxybenzyl bromide (1.1 g, 4.3 mmol) and K2CO3 (8.6 mmol) in 25 ml of THF/HMPA (1:1) is stirred overnight. The reaction is worked up by diluting with ether, washing with water, drying over Na2SO4, and solvent removed to yield 3-phenoxybenzyl 2-(2benzothienyl)-3-methylbutanoate which can be further purified by preparing thin layer chromatography eluting with 5 percent ether/hexane.

後処理

  1. washwashing with water
  2. dry with materialdrying over Na2SO4, and solvent
  3. customremoved

出典と根拠

ORDレコード
ord-d94f0e1a4a804ee5b7e4f30bc6605920
出典データセット
uspto-grants-1980_09
特許番号
US04224330

関連ノート

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