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Phosphorus oxychloride → Ethyl 3-(4-iodophenyl)-3-chloro-2-ethoxycarbonylacrylate

HRID 1740083
ノート
印刷プレビュー

反応式

HRID 1740083 の反応式
[I:1][C:2]1[CH:20]=[CH:19][C:5]([C:6]([CH:8]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:9]([O:11][CH2:12][CH3:13])=[O:10])=O)=[CH:4][CH:3]=1.C(N(C(C)C)CC)(C)C.P(Cl)(Cl)([Cl:32])=O>>[I:1][C:2]1[CH:20]=[CH:19][C:5]([C:6]([Cl:32])=[C:8]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:4][CH:3]=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

4

反応物 3

HCID 24813Phosphorus oxychlorideHCID 81531DiisopropylethylamineHCID 53643535Diethyl 4-iodobenzoylmalonate

生成物 1

HCID 21837631Ethyl 3-(4-iodophenyl)-3-chloro-2-ethoxycarbonylacrylate

反応条件

温度
100 °C

実験手順

A mixture of 28.3 g of diethyl 4-iodobenzoylmalonate, 14.6 g of diisopropylethylamine and 20 ml of phosphorus oxychloride was stirred at 100° C. for 2 hours and then poured over ice. The reaction mixture was extracted with diethyl ether, and the extract was dried over magnesium sulfate, treated with activated carbon, filtered and then concentrated at atmospheric pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to give 20.14 g of the title compound as a pale yellow liquid.

後処理

  1. additionpoured over ice
  2. extractionThe reaction mixture was extracted with diethyl ether
  3. dry with materialthe extract was dried over magnesium sulfate
  4. additiontreated with activated carbon
  5. filtrationfiltered
  6. concentrationconcentrated at atmospheric pressure
  7. customThe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1)

出典と根拠

ORDレコード
ord-6514158aa5f5406ba72b8477e8bafc5c
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05968967

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