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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ammonia → 2,4,6-Cycloheptatrien-1-one, 2-amino-7-bromo-

HRID 2052376
노트
인쇄 미리보기

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HRID 2052376 반응식
[Br:1][C:2]1[C:8](=[O:9])[C:7](OC)=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH3:12]>CO>[NH2:12][C:7]1[C:8](=[O:9])[C:2]([Br:1])=[CH:3][CH:4]=[CH:5][CH:6]=1
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 5711302-Bromo-7-methoxytropone

생성물 1

HCID 373462,4,6-Cycloheptatrien-1-one, 2-amino-7-bromo-

시약·촉매·용매 1

HCID 887Methanol용매

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온도
80 °C

실험 절차

A solution of 7-bromo-2-methoxy-2,4,6-cycloheptatrien-1-one [1.0 g, described by T. Nozol et al., Proc. Japan Acad., 27, 556-60 (1951), (CA 46, 7560c)] in methanol (30 ml) is cooled to -20° C. and saturated with gaseous ammonia. The reaction mixture is heated in a pressure bottle at 80° C. for four hours and cooled to -70° C. The bottle is opened and the solvent is removed under reduced pressure. The residue is boiled with ethyl acetate and the ethyl acetate extract is evaporated to give 2-amino-7-bromo-2,4,6-cycloheptatrien-1-one.

후처리

  1. temperaturecooled to -70° C
  2. customthe solvent is removed under reduced pressure
  3. extractionthe ethyl acetate extract
  4. customis evaporated

출처 및 근거

ORD 기록
ord-40620e5aea5d4061bacb08c1ad20e574
출처 데이터셋
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04183955

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