Hydrochloric Acid → 1,2,3,4-Tetrahydro-4-methoxy-1-naphthylurea
反応式
[OH:1][CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]([NH:12][C:13]([NH2:15])=[O:14])[CH2:4][CH2:3]1.[H-].[Na+].[CH3:18]I.Cl>CN(C)C=O>[CH3:18][O:1][CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]([NH:12][C:13]([NH2:15])=[O:14])[CH2:4][CH2:3]1参加物
6
実験手順
A 2.0 g sample of 1,2,3,4-tetrahydro-4-hydroxy-1-naphthylurea (cis/trans) is stirred in 10 ml of dry dimethylformamide and one equivalent of sodium hydride in mineral oil added at 0° C under a nitrogen atmosphere. After the addition is completed, 1.2 equivalents of methyl iodide is added and the reaction mixture stirred overnight. The mixture is carefully poured on ice, neutralized with hydrochloric acid and the title compound collected by filtration. Evaporation of the filtrate to dryness and washing the residue with water affords additional title compound.
後処理
- additionAfter the addition
- additionThe mixture is carefully poured on ice
- filtrationthe title compound collected by filtration
- customEvaporation of the filtrate to dryness
- washwashing the residue with water
出典と根拠
- ORDレコード
- ord-7e3a9aa6ebad4457a285fc2d2149992a
- 出典データセット
- uspto-grants-1978_05
- 特許番号
- US04089976
反応ノート
読み込み中…