反応式
Cl[CH2:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=1.[CH3:13][NH2:14]>C(O)C>[CH3:13][NH:14][CH2:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=1参加物
4
実験手順
17.6 g of 1-chloromethyl-naphthalene in 40 ml of absolute ethanol is added, dropwise, at 0° to 5°, to 100 ml of a 33% solution of methylamine in absolute ethanol. The mixture is allowed to stand overnight and is then evaporated. The residue is taken up in a little chloroform and washed with 100 ml of 1 N sodium hydroxide solution and with water. The organic phase is dried and evaporated to dryness. The residue is distilled at 0.01 Torr to obtain the heading compound as main fraction, b.p. 85°-87°.
後処理
- customat 0° to 5°
- customis then evaporated
- washwashed with 100 ml of 1 N sodium hydroxide solution and with water
- customThe organic phase is dried
- customevaporated to dryness
- distillationThe residue is distilled at 0.01 Torr
- customto obtain the heading compound as main fraction, b.p. 85°-87°
出典と根拠
- ORDレコード
- ord-be20ca3302fa4fb6bd3a91c49836586f
- 出典データセット
- uspto-grants-1981_08
- 特許番号
- US04282251
関連ノート
読み込み中…