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

HRID 428229
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인쇄 미리보기

반응식

HRID 428229 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 443297Hydroxyamine hydrochlorideHCID 11380407Methyl 4-iodosalicylate

생성물 1

HCID 18357907N,2-dihydroxy-4-iodobenzamide

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

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.

후처리

  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.

출처 및 근거

ORD 기록
ord-181262a53bed48bc836e25305db4dee8
출처 데이터셋
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06313162B1

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