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Hydrochloric Acid → 3-n-Butylamino-4-chloro-5-methylsulfinylbenzoic acid

HRID 1606622
ノート
印刷プレビュー

反応式

HRID 1606622 の反応式
[NH2:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([S:12]([CH3:14])=[O:13])[C:10]=1[Cl:11])[C:5]([OH:7])=[O:6].S(=O)(=O)(O)O.Cl>C(O)CCC>[CH2:3]([NH:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([S:12]([CH3:14])=[O:13])[C:10]=1[Cl:11])[C:5]([OH:7])=[O:6])[CH2:2][CH2:10][CH3:9]
参加物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 1118Sulfuric AcidHCID 215439723-Amino-4-chloro-5-methylsulfinylbenzoic acid

生成物 1

HCID 543482303-n-Butylamino-4-chloro-5-methylsulfinylbenzoic acid

試薬・触媒・溶媒 1

HCID 2631-Butanol溶媒

実験手順

A solution of 3-amino-4-chloro-5-methylsulfinylbenzoic acid (4.67 g.; 0.02 mole) in n-butanol (150 ml.) containing concentrated sulfuric acid (2 ml.) is refluxed for 48 hours in a Soxhlet extractor containing type 4A molecular sieves (100 g.). The solvent is distilled at reduced pressure and the residue is treated with water (50 ml.), 10N sodium hydroxide (20 ml.) and ethanol (20 ml.) and refluxed for 1 hour to hydrolyze any butyl ester which may have formed. The reaction mixture is cooled and acidified with dilute hydrochloric acid to give 3-n-butylamino-4-chloro-5-methylsulfinylbenzoic acid which melts at 158° C. after recrystallization from ethanol and water.

後処理

  1. temperatureis refluxed for 48 hours in a Soxhlet extractor
  2. distillationThe solvent is distilled at reduced pressure
  3. additionthe residue is treated with water (50 ml.), 10N sodium hydroxide (20 ml.) and ethanol (20 ml.)
  4. temperaturerefluxed for 1 hour
  5. custommay have formed
  6. temperatureThe reaction mixture is cooled

出典と根拠

ORDレコード
ord-3c790168f9544381a0a9d4da457576ad
出典データセット
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03953476

反応ノート

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