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Hydrochloric Acid → 1,4-Dihydro-3-hydroxymethyl-5-methyl-8-nitro-4-oxoquinoline

HRID 613564
노트
인쇄 미리보기

반응식

HRID 613564 반응식
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[C:8]2[C:3]=1[C:4](=[O:15])[CH:5]=[CH:6][NH:7]2.[O:16]1COCO[CH2:17]1.Cl>O1CCOCC1>[OH:16][CH2:17][C:5]1[C:4](=[O:15])[C:3]2[C:8](=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=[CH:11][C:2]=2[CH3:1])[NH:7][CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 80811,3,5-TrioxaneHCID 195926861,4-Dihydro-5-methyl-8-nitro-4-oxoquinoline

생성물 1

HCID 195924831,4-Dihydro-3-hydroxymethyl-5-methyl-8-nitro-4-oxoquinoline수율 75.6%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

반응 조건

온도
100 °C

실험 절차

To a stirred mixture of 1,4-dihydro-5-methyl-8-nitro-4-oxoquinoline (1.5 g) and 1,3,5-trioxane (3.31 g) in dioxane (15 ml) was added conc. hydrochloric acid (30 ml), and the mixture was stirred at 100° C. overnight. The mixture was evaporated in vacuo, and the residue was treated with acetonitrile to give 1,4-dihydro-3-hydroxymethyl-5-methyl-8-nitro-4-oxoquinoline (1.3 g).

후처리

  1. customThe mixture was evaporated in vacuo
  2. additionthe residue was treated with acetonitrile

출처 및 근거

ORD 기록
ord-3043f2e64ca143c4b1cbb15485cb5a33
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06008230

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