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Water → Ethyl 2-(4-bromo-2-chlorophenoxy)acetate

HRID 898539
ノート
印刷プレビュー

反応式

HRID 898539 の反応式
CCN(C(C)C)C(C)C.[Br:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([Cl:18])[CH:12]=1.Br[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22].O>CN(C=O)C>[Br:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22])=[C:13]([Cl:18])[CH:12]=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

6

反応物 4

HCID 962WaterHCID 7748Ethyl bromoacetateHCID 198594-Bromo-2-chlorophenolHCID 81531Diisopropylethylamine

生成物 1

HCID 4508433Ethyl 2-(4-bromo-2-chlorophenoxy)acetate

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
100 °C

実験手順

14.5 mL (83.242 mmol) Hünig base was added to a solution of 7.800 g (37.222 mmol) 4-bromo-2-chlorophenol and 4.70 mL (41.537 mmol) ethyl bromoacetate in 100 mL DMF and the mixture was stirred for 4 h at 100° C. The reaction mixture was combined with water and exhaustively extracted with EtOAc. The combined org. phases were washed with saturated aqueous sodium bicarbonate, water and saturated aqueous NaCl, dried over sodium sulphate and evaporated down i. vac. The crude product was used in the next reaction step without any further purification.

後処理

  1. extractionexhaustively extracted with EtOAc
  2. washphases were washed with saturated aqueous sodium bicarbonate, water and saturated aqueous NaCl
  3. dry with materialdried over sodium sulphate
  4. customevaporated down i
  5. customThe crude product was used in the next reaction step without any further purification

出典と根拠

ORDレコード
ord-db4923892c22486e904a16a501c48049
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07351719B2

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