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Isopropylamine → N-[2-[(3,4-Dichlorophenyl)thio]ethyl]-2-propanamine, hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Isopropylamine | HCID 6363 | — |
| 反応物 | Methanesulfonic Acid [2-[(3,4-dichlorophenyl)thio]ethyl]ester | HCID 14050283 | — |
| 生成物 | N-[2-[(3,4-Dichlorophenyl)thio]ethyl]-2-propanamine, hydrochloride | HCID 13655055 | — |
反応手順
A solution of 151.46 g (0.548 mole) of methanesulfonic acid[2-[(3,4-dichlorophenyl)thio]ethyl]ester in 100 ml of isopropylamine was heated overnight in a bomb at 100° C. The isopropylamine was removed in a rotary evaporator and the residue partitioned between chloroform and 5% sodium hydroxide. The chloroform was removed by rotary evaporator to give an oil, the free base of the title compound. The oil was dissolved in methanol and converted to the hydrochloride salt with ethereal hydrogen chloride. Recrystallization of the salt from methanol-diethyl ether gave 101.53 g (61.6%) of white crystalline product, m.p. 132°-133.5° 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-e9ac2303bc5d496eaac98b7e1bc15dcc |
| 出典メモ | uspto-grants-1988_02 |