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Hydrochloric Acid → 2-(Benzyloxy)-5-chlorobenzoic acid

HRID 614817
ノート
印刷プレビュー

反応式

HRID 614817 の反応式
[CH2:1]([O:8][C:9]1[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][C:10]=1[C:11]([O:13]CC1C=CC=CC=1)=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].Cl>CO>[CH2:1]([O:8][C:9]1[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][C:10]=1[C:11]([OH:13])=[O:12])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=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 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 13026912Benzyl 2-benzyloxy-5-chlorobenzoate

生成物 1

HCID 33011592-(Benzyloxy)-5-chlorobenzoic acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
10 °C

実験手順

A mixture of 5-chlorosalicyclic acid (7.7 g), benzyl chloride (10.35 ml), anhydrous potassium carbonate (6.2 g), and dry sulpholane (100 ml) was stirred and heated in an oil bath at 120° C. for 20 hours. The yellow solution was cooled and poured into a mixture of ice and water (300 ml) and the mixture was acidified to pH 1 by treatment with concentrated hydrochloric acid. The brown oil which separated was extracted with diethyl ether (400 ml), the ether extract was washed with aqueous sodium carbonate solution (2N; 150 ml), dried over magnesium sulphate, and evaporated, to give a white solid (16 g), m.p 45°-50° C., consisting mainly of benzyl 2-benzyloxy-5-chlorobenzoate. This material was heated at reflux with aqueous sodium hydroxide solution (2N; 100 ml) for 3 hours. The mixture was then treated with methanol (40 ml) and heated at reflux for 6 hours. The resulting solution was neutralised to pH 7 by treatment with hydrochloric acid (2N), then concentrated under reduced pressure, acidified to pH 5 by treatment with hydrochloric acid (2N) and cooled to 10° C. The separated solid was filtered off and washed with a mixture of ice and water and recrystallized from acetic acid (100 ml) (filtering off some insoluble material ) to give 2-benzyloxy-5-chlorobenzoic acid (5.23 g), m.p. 113°-115° C.

後処理

  1. temperatureThis material was heated
  2. temperatureheated
  3. temperatureat reflux for 6 hours
  4. concentrationconcentrated under reduced pressure
  5. filtrationThe separated solid was filtered off
  6. washwashed with a mixture of ice and water
  7. customrecrystallized from acetic acid (100 ml) (
  8. filtrationfiltering off some insoluble material )

出典と根拠

ORDレコード
ord-972334ac98704d30874a22dc0b36813d
出典データセット
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04146631

反応ノート

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