戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1153869作成日:2026年10月26日

Butyl isocyanate → 2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamide

https://huagongshe.com/reaction/1153869

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl isocyanateHCID 8110—
反応物2-(Chloromethyl)benzenesulfonamideHCID 13364627—
触媒Diazabicyclo(2.2.2)octaneHCID 136165—
溶媒O-XyleneHCID 7237—
生成物2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamideHCID 1363188774.8%

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°. 1H nmr δCDCl3TMS 9.5-8.1 (brds), 8.05-7.10 (m), 6.28 (t, J=2 Hz), 4.91 (s), 3.25-2.95 (m), 1.70-0.70 (m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04486589
出典データセットuspto-grants-1984_12
ORD IDord-10390e26897849d38b250841db16aacf
出典メモuspto-grants-1984_12