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Butyl isocyanate → 2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Butyl isocyanate | HCID 8110 | — |
| 反応物 | 2-(Chloromethyl)benzenesulfonamide | HCID 13364627 | — |
| 触媒 | Diazabicyclo(2.2.2)octane | HCID 136165 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamide | HCID 13631887 | 74.8% |
反応手順
A mixture of 2-(chloromethyl)benzenesulfonamide (13.2 g, 64 mmol) and butyl isocyanate (7.0 g, 71 mmol) in xylene (80 ml) was contacted with diazabicyclo[2.2.2]octane (0.25 g) and heated to reflux for 5.0 hrs. Volatiles were removed under vacuum and the residue was treated with 0.5N NaOH (200 ml) and extracted with ethyl acetate (75 ml). The aqueous layer was separated, chilled, acidified (pH 4) with hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4), and evaporated to give 14.6 g of white solid. A sample was recrystallized from toluene to give m.p. 104°-106°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04723990 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-96b36f56b2bf4e2fa59c2f023ae48e35 |
| 出典メモ | uspto-grants-1988_02 |