4-Bromo-1-naphthylamine → 1-Bromo-4-isothiocyanatonaphthalene
反応式
[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([NH2:12])=[CH:4][CH:3]=1.N1([C:18](N2C=CN=C2)=[S:19])C=CN=C1>ClCCl>[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([N:12]=[C:18]=[S:19])=[CH:4][CH:3]=1参加物
4
実験手順
To a solution of 1-bromo-4-aminonapthalene (2.6 g, 12 mmol) in dichloromethane (45 mL) was added di(1H-imidazol-1-yl)methanethione (2.1 g, 12 mmol). The reaction was allowed to stir for 16 h, at which point the reaction was concentrated to give a gray solid. The solid was slurried in 50% EtOAc/hexanes and filtered through a pad of silica gel, rinsing with 400 mL 50% EtOAc/hexanes. The solution was concentrated to give 1-bromo-4-isothiocyanatonaphthalene as a gray solid, which was used without further purification.
後処理
- concentrationwas concentrated
- customto give a gray solid
- filtrationfiltered through a pad of silica gel
- washrinsing with 400 mL 50% EtOAc/hexanes
- concentrationThe solution was concentrated
出典と根拠
- ORDレコード
- ord-c13ad54d628945bdbf6ed5cf456ba6e9
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07776869B2
反応ノート
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