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HRID 343748생성일: 2026년 10월 23일

4-Methyl-5-nitrosaccharin → 4-Methyl-5-aminosaccharin

https://huagongshe.com/ko/reaction/343748

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl-5-nitrosaccharinHCID 15334534—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매WaterHCID 962—
생성물4-Methyl-5-aminosaccharinHCID 70187691—

반응 조건

온도45 °C

반응 단계

33.6 g (0.13 mol) of 4-methyl-5-nitro-1,1,3-trioxo-2,3-dihydro-1λ6 benz[d]isothiazole are dissolved in 1.2 l of water with warming to 45° C. and 5 g of Pd/C (10 percent on active carbon) are added. Hydrogen gas is then passed in with vigorous stirring (pressureless hydrogenation). 9 l of H2 are absorbed in the course of 4.5 hours. After cooling to 25° C., the catalyst is filtered off, and the filtrate is concentrated to a volume of 200 ml (on a Rotavapor) and then acidified to pH 1. The deposited precipitate is filtered off with suction, washed with water and dried under reduced pressure at 50° C. 23.4 g (0.11 mol=85% of theory) of a white solid of m.p.: 272°-273° C. are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05863864
출처 데이터셋uspto-grants-1999_01
ORD IDord-c2a0168562554394973e6eb710a292fe
출처 메모uspto-grants-1999_01