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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Dimethylamino-2-nitrobenzaldehyde → 2-Nitro-4-dimethylaminobenzaldoxime

HRID 918555
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인쇄 미리보기

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HRID 918555 반응식
[N+:1]([C:4]1[CH:11]=[C:10]([N:12]([CH3:14])[CH3:13])[CH:9]=[CH:8][C:5]=1[CH:6]=O)([O-:3])=[O:2].Cl.[NH2:16][OH:17].C([O-])(=O)C.[Na+]>C(O)C.O>[N+:1]([C:4]1[CH:11]=[C:10]([N:12]([CH3:14])[CH3:13])[CH:9]=[CH:8][C:5]=1[CH:6]=[N:16][OH:17])([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 2913524-Dimethylamino-2-nitrobenzaldehydeHCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium Acetate

생성물 1

HCID 867337652-Nitro-4-dimethylaminobenzaldoxime수율 71%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

9.7 parts of 2-nitro-4-dimethylaminobenzaldehyde is dissolved in 50 parts of ethyl alcohol and a solution of 4.1 parts of hydroxylamine hydrochloride and 5 parts of sodium acetate in water is added. After the mixture has been boiled for one hour it is suction filtered. 7.5 parts (71% of theory) of 2-nitro-4-dimethylaminobenzaldoxime is obtained having a melting point of 140° to 143°C: ##SPC18##

후처리

  1. filtrationfiltered

출처 및 근거

ORD 기록
ord-b3a3dbe3cf6d462bbd41fda1c0ff0051
출처 데이터셋
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03971821

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