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Acetic Anhydride → HCID 13435388, 화합물

HRID 904819
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HRID 904819 반응식
[N:1](=[C:3]1[CH2:12][CH2:11][C:10]2[C:5](=[CH:6][C:7]([O:13][CH3:14])=[CH:8][CH:9]=2)[C:4]1=[O:15])O.[C:16](OC(=O)C)(=[O:18])[CH3:17]>[Pd]>[C:16]([NH:1][CH:3]1[CH2:12][CH2:11][C:10]2[C:5](=[CH:6][C:7]([O:13][CH3:14])=[CH:8][CH:9]=2)[C:4]1=[O:15])(=[O:18])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 73667394HCID 73667394, 화합물

생성물 1

HCID 13435388HCID 13435388, 화합물

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

A mixture of 2-oximino-7-methoxy-3,4-dihydronaphthalen-1(2H)-one (8.7 gm, 0.04 m), palladium on carbon (10%, 1 gm) tetrahydrofuran (150 ml) and acetic anhydride (25 ml) was hydrogenated on a Parr apparatus for 3 hours. The catalyst was filtered, and the solvents were removed under reduced pressure to yield the product as an oil, which was used in the next step without further purification.

후처리

  1. filtrationThe catalyst was filtered
  2. customthe solvents were removed under reduced pressure

출처 및 근거

ORD 기록
ord-cd33c48e43c74e399e20dc0c16a9f271
출처 데이터셋
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04420480

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