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2-Bromoethanol → 4-Methoxybenzyl 4-(2-hydroxyethoxy)benzoate

HRID 489054
ノート
印刷プレビュー

反応式

HRID 489054 の反応式
[OH:1][C:2]1[CH:19]=[CH:18][C:5]([C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)=[O:7])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:27][CH2:28][OH:29]>CN(C)C=O>[OH:29][CH2:28][CH2:27][O:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)=[O:7])=[CH:18][CH:19]=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

5

反応物 3

HCID 108982-BromoethanolHCID 11430Potassium CarbonateHCID 12119266Benzoic acid, 4-hydroxy-, (4-methoxyphenyl)methyl ester

生成物 1

HCID 220358874-Methoxybenzyl 4-(2-hydroxyethoxy)benzoate

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
80 °C

実験手順

To a solution of 4methoxybenzyl 4-hydroxybenzoate (7.0 g, 27 mmole) in dry N,N-dimethylformamide (50 ml) was added potassium carbonate (4.15 g, 30 mmole) and 2-bromoethanol. The mixture was stirred 48 hours at 80° C., evaporated under reduced pressure and ethyl acetate and water were added. The organic phase was washed five times with water and dried with sodium sulfate. The solution was evaporated under reduced pressure and the product was isolated by silica gel column chromatography with hexane/ethyl acetate.

後処理

  1. customevaporated under reduced pressure and ethyl acetate and water
  2. additionwere added
  3. washThe organic phase was washed five times with water
  4. dry with materialdried with sodium sulfate
  5. customThe solution was evaporated under reduced pressure
  6. customthe product was isolated by silica gel column chromatography with hexane/ethyl acetate

出典と根拠

ORDレコード
ord-56de8da4c96c4ccfa0e5cd1e23012a6e
出典データセット
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06974802B2

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