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Hydrochloric Acid → 2-Chloro-6-hydroxybenzoic acid

HRID 1885966
ノート
印刷プレビュー

反応式

HRID 1885966 の反応式
Cl.[Cl:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7](N)[C:8]=1[C:9]([OH:11])=[O:10].Cl.N([O-])=[O:15].[Na+]>O>[Cl:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]([OH:15])[C:8]=1[C:9]([OH:11])=[O:10]
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 23668193Sodium NitriteHCID 53444447HCID 53444447、化合物

生成物 1

HCID 925912-Chloro-6-hydroxybenzoic acid収率 44.7%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

反応条件

温度
5 °C

実験手順

A stirred suspension of 10.0 grams (0.048 mole) of 6-chloroanthranilic acid hydrochloride and 100 mL of concentrated hydrochloric acid in 200 mL of water was cooled to 5° C., and a solution of 3.5 grams (0.050 mole) of sodium nitrite in 50 mL of water was added dropwise during a 10 minute period. Upon completion of addition, the reaction mixture was warmed to 90° C. where it was stirred for about 10 minutes. The reaction mixture was cooled to ambient temperature and was filtered. The filter cake was washed with cold heptane and dried to yield 3.7 grams of 6-chlorosalicylic acid. The nmr spectrum was consistent with the proposed structure.

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

後処理

  1. additionUpon completion of addition
  2. temperaturethe reaction mixture was warmed to 90° C. where it
  3. temperatureThe reaction mixture was cooled to ambient temperature
  4. filtrationwas filtered
  5. washThe filter cake was washed with cold heptane
  6. customdried

出典と根拠

ORDレコード
ord-4fc6ca6a540947d78b46c25c4aec1019
出典データセット
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05149357

反応ノート

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