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Hydroxyamine hydrochloride → HCID 14012586, 화합물

HRID 652857
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반응식

HRID 652857 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([C:8](=O)[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[F:15])[C:5]([Cl:17])=[CH:4][C:3]=1[O:18][CH3:19].Cl.[NH2:21][OH:22]>N1C=CC=CC=1>[F:15][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1/[C:8](=[N:21]/[OH:22])/[C:6]1[CH:7]=[C:2]([Cl:1])[C:3]([O:18][CH3:19])=[CH:4][C:5]=1[Cl:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 14012557HCID 14012557, 화합물

생성물 1

HCID 14012586HCID 14012586, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A mixture of 2,5-dichloro-4-(2-fluorobenzoyl)anisole (3 g) and hydroxylamine hydrochloride (1.4 g) in pyridine (25 ml) is refluxed for several hours until no ketone remains. The pyridine is removed under high vacuum and the residue diluted with water, then extracted with chloroform. The chloroform solution is dried and the chloroform removed to give a solid which is recrystallized from ether to afford (z)-2'-fluoro-2,5-dichloro-4-methoxybenzophenone oxime, mp 188° C.

후처리

  • customThe pyridine is removed under high vacuum
  • additionthe residue diluted with water
  • extractionextracted with chloroform
  • dry with materialThe chloroform solution is dried
  • customthe chloroform removed
  • customto give a solid which
  • customis recrystallized from ether
  • 출처 및 근거

    ORD 기록
    ord-22b87c8444af41a0b896955574bf3116
    출처 데이터셋
    uspto-grants-1987_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04673746

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