反応式
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[CH2:4]Cl.[NH3:11]>C1C=CC=CC=1>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[CH2:4][NH2:11]参加物
4
反応条件
- 温度
- 100 °C
実験手順
An autoclave was charged with 89.0 g. (0.5 mole) of 2-chloro-6-fluorobenzyl chloride, 170.0 g. (10 mole) ammonia and 50 ml. benzene. The reaction vessel was sealed and the contents heated at 100° C. for 15 hours. The excess ammonia was carefully evaporated off from the cooled contents of the autoclave with a stream of nitrogen. The residue was washed with water, and the organic phase after drying with anhydrous MgSO4, fractionated to afford 72.4 g. (90%) of product as a clear liquid; b.p. 99°-100° C./20 mm; NMR (CDCl3) δ 1.46 (s, 2H); 3.88 (d, 2H); 7.00 (m, 3H).
後処理
- additionAn autoclave was charged with 89.0 g
- customThe reaction vessel was sealed
- customThe excess ammonia was carefully evaporated off from the cooled contents of the autoclave with a stream of nitrogen
- washThe residue was washed with water
- dry with materialthe organic phase after drying with anhydrous MgSO4
- customto afford 72.4 g
出典と根拠
- ORDレコード
- ord-d162db78788f4b4f982c0b9e20eafc34
- 出典データセット
- uspto-grants-1978_07
- 特許番号
- US04098787
関連ノート
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