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Acetic Anhydride → HCID 9859076, 화합물

HRID 904821
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인쇄 미리보기

반응식

HRID 904821 반응식
[N:1](=[C:3]1[CH2:12][CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4]1)O.[C:13](OC(=O)C)(=[O:15])[CH3:14].[O:20]1CCCC1>[Pd]>[C:13]([NH:1][CH:3]1[CH2:12][CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]1=[O:20])(=[O:15])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7918Acetic AnhydrideHCID 8028TetrahydrofuranHCID 71437055HCID 71437055, 화합물

생성물 1

HCID 9859076HCID 9859076, 화합물

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

A slurry of 2-oximino-3,4-dihydronaphthalen-[1(2H)-one (8.75 gm, 0.05 m) acetic anhydride (25 ml), tetrahydrofuran (150 ml) and Pd/C (10%, 500 mg) was hydrogenated on a Parr apparatus for 3 hours. The catalyst was removed by filtration through diatomaceous earth. The organic solvents were evaporated under reduced pressure (20 mm) to yield the product as an oil, which was used in the next step without further purification.

후처리

  1. customThe catalyst was removed by filtration through diatomaceous earth
  2. customThe organic solvents were evaporated under reduced pressure (20 mm)

출처 및 근거

ORD 기록
ord-74327dc6bb1e4c6e844b4c077bc9bd0a
출처 데이터셋
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04420480

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