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Methylamine → 6-Bromo-2-methylamino-1-nitronaphthalene

HRID 1494336
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HRID 1494336 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([N+:12]([O-:14])=[O:13])=[C:7](OC)[CH:6]=[CH:5]2.[CH3:17][NH2:18]>CN(C)C=O>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([N+:12]([O-:14])=[O:13])=[C:7]([NH:18][CH3:17])[CH:6]=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6329Methylamine2회HCID 220971876-Bromo-2-methoxy-1-nitronaphthalene

생성물 1

HCID 198278026-Bromo-2-methylamino-1-nitronaphthalene

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of 6-bromo-2 methoxy-1-nitronaphthalene (5.64 g, 20 mmol) in 100 ml of dry N,N-dimethylformamide saturated with methylamine was stirred in a stoppered flask at 80° C. for 4 h. During the reaction period the mixture was saturated twice with a further quantity of methylamine. The cooled mixture was poured into 1 l of ice/water. After stirring for 1 h, the orange solid was collected by filtration and washed with water, and dried in vacuo over phosphorus pentoxide affording 5.43 g (96%) of the title compound. M.p. 169°-170° C.; 1H-NMR (CDCl3): 3.11 (d, J=5 Hz, 3H, CH3), 7.00 (d, J=9 Hz, 1H, ArH), 7.45- 7.78 (m, 3H, ArH), 8.60 (d, J =9 Hz, 1H, ArH), 8.7 (broad, 1H, NH).

후처리

  1. customDuring the reaction period the mixture
  2. filtrationthe orange solid was collected by filtration
  3. washwashed with water
  4. dry with materialdried in vacuo over phosphorus pentoxide affording 5.43 g (96%) of the title compound

출처 및 근거

ORD 기록
ord-b837bca62c2f40b098ced3df8e11a9d3
출처 데이터셋
uspto-grants-1991_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05026704

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