戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 5592作成日:2026年10月23日

Ammonia → 1-Benzylindole

https://huagongshe.com/ja/reaction/5592

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物IndoleHCID 798—
反応物Benzyl ChlorideHCID 7503—
反応物Sodium amideHCID 24533—
反応物SodiumHCID 5360545—
溶媒Diethyl EtherHCID 3283—
生成物1-BenzylindoleHCID 96913—

反応手順

To a stirred mixture of sodium amide (prepared from 19.6 g, 0.85 mole of sodium and a few mg of Fe(NO3)3 -9H2O) and 800 mL of liquid NH3 (a dry ice condenser was used) was added a solution of 100 g (0.85 mole) of indole in 250 mL of dry ether during 15 minutes. The mixture was stirred for 30 minutes and then a solution of 107.8 g (0.85 mole) of benzyl chloride in 100 mL of dry ether was added during 30 minutes. The ammonia was allowed to evaporate overnight. The sides of the flask were washed down with MeOH and then 500 mL of H2O was added. The mixture was extracted with ether (2×500 mL). The combined ether extracts were washed with 250 mL of H2O and dried over MgSO4. The solvent was evaporated. The residue was distilled at 2 mm: fr 1, b.p. 172°- 183°, fr II, b.p. 183°-186°, 5 g; fr III, b.p. 186°-187°, 10.9 g; fr IV, b.p. 187°-191°, 121.8 g; fr V, b.p. 191°-197°, 13.9 g. Fractions III-V solidified upon standing several hours. Fraction IV had m.p. 42°-43°. Fraction III was crystallized from aqueous MeOH giving 9.9 g of colorless needles, m.p. 42.5°-43.5°. Fraction V was crystallized from aqueous MeOH giving 11.6 g of colorless needles, m.p. 43°-45.5°. The total yield was 143.3 g (81.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05245046
出典データセットuspto-grants-1993_09
ORD IDord-6e955e2991c44b43badb9a9ccdf6b729
出典メモuspto-grants-1993_09