Thionyl Chloride → Methyl 1-chloroindan-4-carboxylate

HRID 1606721

反応式

HRID 1606721 の反応式
O[CH:2]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11]([O:13][CH3:14])=[O:12])[C:5]=2[CH2:4][CH2:3]1.S(Cl)([Cl:17])=O>>[Cl:17][CH:2]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11]([O:13][CH3:14])=[O:12])[C:5]=2[CH2:4][CH2:3]1

参加物

3

実験手順

In 6 ml. of chllroform is dissolved 5.7 g. of methyl 1-hydroxyindan-4-carboxylate and, under cooling with ice, the solution is stirred. Then, 3 ml. of thionyl chloride is added dropwise and, after the dropwise addition has been completed, the mixture is further stirred under cooling with ice for one hour. Then, the solvent and the excess thionyl chloride are distilled off under reduced pressure. The residue obtained is purified by column chromatography on silica gel (500 g. silica gel; eluant: chloroform). The procedure gives methyl 1-chloroindan-4-carboxylate as an oily product.

後処理

  1. dissolutionof chllroform is dissolved 5.7 g
  2. additionafter the dropwise addition
  3. stirringthe mixture is further stirred
  4. temperatureunder cooling with ice for one hour
  5. distillationThen, the solvent and the excess thionyl chloride are distilled off under reduced pressure
  6. customThe residue obtained
  7. customis purified by column chromatography on silica gel (500 g. silica gel; eluant: chloroform)

出典と根拠

ORDレコード
ord-49d482482cf3431abc7d24e93cc534d1
出典データセット
uspto-grants-1976_04
特許番号
US03953500

関連ノート

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