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Dimethyl Sulfate → 6-Bromo-2-methoxy-N-methyl-1-naphthamide

HRID 480452
ノート
印刷プレビュー

反応式

HRID 480452 の反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([C:12]([NH:14][CH3:15])=[O:13])=[C:7]([OH:16])[CH:6]=[CH:5]2.[CH3:17]OS(OC)(=O)=O.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([C:12]([NH:14][CH3:15])=[O:13])=[C:7]([O:16][CH3:17])[CH:6]=[CH:5]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 187690866-Bromo-2-hydroxy-N-methyl-1-naphthamide

生成物 1

HCID 187690686-Bromo-2-methoxy-N-methyl-1-naphthamide

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
60 °C

実験手順

A mixture of 6-Bromo-2-hydroxy-N-methyl-1-naphthamide (1.20 g), dimethylsulfate (0.49 mL), and powdered K2CO3 (1.18 g) in anhydrous DMF (10 mL) was heated at 60° C. for 30 min. After dilution with 1N HCl, the resulting mixture was extracted with Ethyl acetate. The combined organic layers were washed with water and brine followed by drying over MgSO4. After removal of the solvent in vacuo, the residue was washed with hexane-AcOEt (1:1) to give the title compound (1.21 g) as a colorless powder.

後処理

  1. extractionAfter dilution with 1N HCl, the resulting mixture was extracted with Ethyl acetate
  2. washThe combined organic layers were washed with water and brine
  3. dry with materialby drying over MgSO4
  4. customAfter removal of the solvent in vacuo
  5. washthe residue was washed with hexane-AcOEt (1:1)

出典と根拠

ORDレコード
ord-a28776cc27d64c1197245c418599af5c
出典データセット
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06649643B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート