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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydroxyamine hydrochloride → HCID 136359213, 화합물

HRID 568609
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반응식

HRID 568609 반응식
[Cl:1][C:2]1[C:16]([Cl:17])=[C:15]([OH:18])[CH:14]=[CH:13][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[F:12])=O.Cl.[NH2:20][OH:21]>N1C=CC=CC=1>[Cl:1][C:2]1[C:16]([Cl:17])=[C:15]([OH:18])[CH:14]=[CH:13][C:3]=1[C:4](=[N:20][OH:21])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[F:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 13015711HCID 13015711, 화합물

생성물 1

HCID 136359213HCID 136359213, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 31.8 g of 2,3-dichloro-4-hydroxy-2'-fluoro-benzophenone and 15.3 g of hydroxylamine hydrochloride in 150 ml of pyridine is refluxed for 64 hours. Thereafter, the pyridine is evaporated under vacuum and a 5% aqueous hydrochloric acid solution is added. The acidified solution is extracted with ethyl acetate and the combined extracts are dried before being concentrated to dryness. The resulting solid is recrystallized from an aqueous ethanol solution to yield the product 2,3-dichloro-4-hydroxy-2'-fluorobenzophenone oxime with a melting point of 168° to 175° C.

후처리

  1. customThereafter, the pyridine is evaporated under vacuum
  2. additiona 5% aqueous hydrochloric acid solution is added
  3. extractionThe acidified solution is extracted with ethyl acetate
  4. customthe combined extracts are dried
  5. concentrationbefore being concentrated to dryness
  6. customThe resulting solid is recrystallized from an aqueous ethanol solution

출처 및 근거

ORD 기록
ord-f8eebe77ca554918b9e2885fe58a1926
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04728662

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