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Benzylamine → N-[2-(Phenylsulfonyl)ethyl]benzenemethanamine hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzylamine | HCID 7504 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | ((2-Chloroethyl)sulphonyl)benzene | HCID 13646 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-[2-(Phenylsulfonyl)ethyl]benzenemethanamine hydrochloride | HCID 13655083 | — |
反応手順
A mixture of 71.90 g (0.352 mole) of 2-chloroethyl phenyl sulfone, 37.45 g (0.350 mole) of benzylamine and 60 ml of triethylamine in 800 ml of acetonitrile was stirred at room temperature for ≈64 hr. The solvent was removed in vacuo and the residue was partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution was dried over magnesium sulfate, and the volume was reduced in vacuo to 300 ml. Methanol was added followed by an excess of ethereal hydrogen chloride. A white precipitate was collected to give 81.30 g (74.5%) of white, crystalline solid, m.p. 211°-213° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04724235 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-81ada1811183440c81eed8afb7279bd4 |
| 出典メモ | uspto-grants-1988_02 |