Sodium Carbonate → 4-(7-Bromo-1,3-benzodioxol-4-yl)-4-methyl-2-oxo-valeric acid-ethyl ester

HRID 2215480ノート

反応式

HRID 2215480 の反応式
[Br:1][C:2]1[C:7]2[O:8][CH2:9][O:10][C:6]=2[C:5]([C:11](O)([CH3:13])[CH3:12])=[CH:4][CH:3]=1.[CH2:15]([O:17][C:18](=[O:26])[C:19]([O:21][Si](C)(C)C)=[CH2:20])[CH3:16].[Sn+6].[Cl-].C(=O)([O-])[O-].[Na+].[Na+]>ClCCl>[CH2:15]([O:17][C:18](=[O:26])[C:19](=[O:20])[CH2:21][C:11]([C:5]1[C:6]2[O:10][CH2:9][O:8][C:7]=2[C:2]([Br:1])=[CH:3][CH:4]=1)([CH3:13])[CH3:12])[CH3:16]

参加物

6

反応物 4

HCID 10340Sodium CarbonateHCID 111168062-Trimethylsilanyloxy-acrylic acid ethyl esterHCID 219488102-(7-Bromobenzo[1,3]dioxol-4-yl)-propan-2-olHCID 178479825HCID 178479825、化合物

生成物 1

HCID 692037914-(7-Bromo-1,3-benzodioxol-4-yl)-4-methyl-2-oxo-valeric acid-ethyl ester収率 129.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-70 °C

実験手順

1.77 g of 2-(7-bromobenzo[1,3]dioxol-4-yl)-propan-2-ol and 2.82 g of 2-trimethylsilyloxy-acrylic acid-ethyl ester (WO 00/32584) in 36 ml of dichloromethane are mixed at −70° C. with 1.10 ml of tin(VI)chloride. It is stirred for 20 minutes at −70° C. and then added to saturated sodium carbonate solution. It is extracted with dichloromethane, washed with water, dried and concentrated by evaporation in a vacuum. 3.15 g of 4-(7-bromo-1,3-benzodioxol-4-yl)-4-methyl-2-oxo-valeric acid-ethyl ester is obtained as a crude product. The latter is reacted for 4 hours at room temperature in 57 ml of a mixture that consists of 1N sodium hydroxide solution in ethanol/water. The batch is added to water, extracted with ether and then the aqueous phase is acidified with hydrochloric acid. It is extracted with ethyl acetate, washed with water, dried with sodium sulfate and concentrated by evaporation in a vacuum. 2.1 g of 4-(7-bromo-1,3-benzodioxol-4-yl)-4-methyl-2-oxo-valeric acid is obtained as a yellow oil.

後処理

  1. extractionIt is extracted with dichloromethane
  2. washwashed with water
  3. customdried
  4. concentrationconcentrated by evaporation in a vacuum

出典と根拠

ORDレコード
ord-f6201d9cc17049aaa18250a07f0cedd9
出典データセット
uspto-grants-2006_09
特許番号
US07109212B2

反応ノート

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