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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905146생성일: 2026년 10월 25일

Sulfuric Acid → Octylmethylamine

https://huagongshe.com/reaction/905146

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물BenzenesulfonamideHCID 7370—
반응물OctylamineHCID 8143—
반응물Sodium HydroxideHCID 14798—
반응물Sodium ethoxideHCID 2723922—
용매O-XyleneHCID 7237—
생성물OctylmethylamineHCID 75538—

반응 단계

523 g of the benzene sulfonamide of octylamine are dissolved in 1500 cc of anhydrous xylene. There are then introduced, with agitation, 835 cc of a 2.4 N ethanolic solution of sodium ethylate. The ethanol is then eliminated by distillation. While agitating the reaction mixture and maintaining its temperature at 100°-110° C., there are introduced over a one hour period 385 cc of methyl sulfate. The resulting mixture is heated at reflux for 4 hours. After cooling, the mineral salts formed are removed by filtration. There are then added to the filtrate 1500 cc of a concentrated aqueous solution of NaOH. The resulting mixture is decanted and the xylenic phase is washed 4 times with 1000 cc of water and then concentrated. The residue obtained is added to a mixture of 1400 g of concentrated sulfuric acid and about 560 g of crushed ice. The resulting mixture is then brought, with agitation, to 160° C. for 16 hours. After cooling, the reaction mixture is poured onto 3 kg of crushed ice and made alkaline by the addition of 3500 cc of a concentrated aqueous solution of NaOH, which is then extracted three times with 2000 cc of ethyl acetate. The organic phase is then washed with water, dried and concentrated under reduced pressure. The residue is distilled and the fraction distilling at 45°-50° C. under 0.2 mm Hg is recovered.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04422853
출처 데이터셋uspto-grants-1983_12
ORD IDord-c76e08a526e640f7a8521b2e203cf81a
출처 메모uspto-grants-1983_12