1-Propanol → 2-Bromo-4-ethylsulfonyl-1-propoxybenzene

HRID 575695ノート

反応式

HRID 575695 の反応式
[CH2:1]([OH:4])[CH2:2][CH3:3].[H-].[Na+].[Br:7][C:8]1[CH:13]=[C:12]([S:14]([CH2:17][CH3:18])(=[O:16])=[O:15])[CH:11]=[CH:10][C:9]=1F.[NH4+].[Cl-]>C1COCC1.CC(=O)OCC>[Br:7][C:8]1[CH:13]=[C:12]([S:14]([CH2:17][CH3:18])(=[O:16])=[O:15])[CH:11]=[CH:10][C:9]=1[O:4][CH2:1][CH2:2][CH3:3]

参加物

7

反応物 4

HCID 10311-PropanolHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 585219752-Bromo-4-(ethylsulfonyl)-1-fluorobenzene

生成物 1

HCID 1180220082-Bromo-4-ethylsulfonyl-1-propoxybenzene収率 52.3%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
0 °C

実験手順

To a solution of n-propanol (224 mg, 3.74 mmol) in THF (10 mL) was added NaH (112 mg, 2.80 mmol, 60% in mineral oil) at 0° C. After stirring at 0° C. for 30 min, 2-bromo-4-(ethanesulfonyl)-1-fluorobenzene (500 mg, 1.87 mmol) was added and the mixture was stirred at room temperature for 4 h. Addition of saturated NH4Cl (10 mL) followed by EA extractive work up gave the title compound (300 mg, yield: 52.3%) which was carried on directly.

後処理

  1. stirringthe mixture was stirred at room temperature for 4 h

出典と根拠

ORDレコード
ord-28661011b23e480f9d4f089803101aa5
出典データセット
uspto-grants-2015_05
特許番号
US09034900B2

反応ノート

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