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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → 2,8-Diacetylamino-1-tetralone

HRID 355946
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인쇄 미리보기

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HRID 355946 반응식
[C:1]([NH:4][C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:14]=1[C:13](=[O:15])[C:12](=[N:16]O)[CH2:11][CH2:10]2)(=[O:3])[CH3:2].[C:18](O)(=[O:20])[CH3:19]>C(OC(=O)C)(=O)C.[Zn]>[C:18]([NH:16][CH:12]1[CH2:11][CH2:10][C:9]2[C:14](=[C:5]([NH:4][C:1](=[O:3])[CH3:2])[CH:6]=[CH:7][CH:8]=2)[C:13]1=[O:15])(=[O:20])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 867509568-Acetylamino-2-hydroxyimino-1-tetralone

생성물 1

HCID 120472982,8-Diacetylamino-1-tetralone

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 7918Acetic Anhydride용매

실험 절차

1 gm of zinc powder was added to a solution of 300 mg of the compound prepared in (2) above dissolved in a mixed solvent of 10 ml of acetic acid and 10 ml of acetic anhydride, and the mixture was stirred for 40 minutes at room temperature. Insoluble substances were removed by filtration and filtrate was concentrated. The residue was recrystallized in ethyl acetate and hexane to obtain 263 mg of the title compound.

후처리

  1. customInsoluble substances were removed by filtration and filtrate
  2. concentrationwas concentrated
  3. customThe residue was recrystallized in ethyl acetate

출처 및 근거

ORD 기록
ord-4f6593ea681143ac8b6e501516b36baf
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05834476

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