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Hydrochloric Acid → N,2-dihydroxy-4-iodobenzamide

HRID 428229
ノート
印刷プレビュー

反応式

HRID 428229 の反応式
[OH:1][C:2]1[CH:11]=[C:10]([I:12])[CH:9]=[CH:8][C:3]=1[C:4](OC)=[O:5].Cl.[NH2:14][OH:15].Cl>[OH-].[Na+]>[OH:15][NH:14][C:4](=[O:5])[C:3]1[CH:8]=[CH:9][C:10]([I:12])=[CH:11][C:2]=1[OH:1]
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 443297Hydroxyamine hydrochlorideHCID 11380407Methyl 4-iodosalicylate

生成物 1

HCID 18357907N,2-dihydroxy-4-iodobenzamide

試薬・触媒・溶媒 1

HCID 14798Sodium Hydroxide溶媒

実験手順

23.3 g (84 mmol) of methyl 2-hydroxy-4-iodobenzoate and 360 ml of sodium hydroxide solution (1 N) are introduced into a three-necked flask under a stream of nitrogen. 8 g (113 mmol) of hydroxylamine hydrochloride are added and the mixture is stirred at room temperature for two hours. The reaction medium is adjusted to pH 7-8 with concentrated hydrochloric acid and the solid is filtered off. The solid is dissolved in ethyl acetate and washed with water, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and evaporated. The residue is triturated from heptane, filtered and dried. 17.6 g (71.5%) of the expected product are collected, with a melting point of 195-6° C.

後処理

  1. filtrationthe solid is filtered off
  2. dissolutionThe solid is dissolved in ethyl acetate
  3. washwashed with water
  4. customthe organic phase is separated out after settling
  5. dry with materialdried over magnesium sulphate
  6. customevaporated
  7. customThe residue is triturated from heptane
  8. filtrationfiltered
  9. customdried
  10. custom17.6 g (71.5%) of the expected product are collected, with a melting point of 195-6° C.

出典と根拠

ORDレコード
ord-181262a53bed48bc836e25305db4dee8
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06313162B1

反応ノート

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