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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 660123생성일: 2026년 10월 27일

2-Methyl-2-nitro-1,3-propanediol → 2-Methyl-2-nitro-1,3-propanediol-di-p-toluenesulfonate

https://huagongshe.com/reaction/660123

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-nitro-1,3-propanediolHCID 6480—
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물TriethylamineHCID 8471—
용매Diethyl EtherHCID 3283—
생성물2-Methyl-2-nitro-1,3-propanediol-di-p-toluenesulfonateHCID 5195535.7%

반응 조건

온도0 °C

반응 단계

To a solution of 2-methyl-2-nitro-1,3-propanediol (80 g, 0.592 mol) and triethylamine (131.8 g, 1.303 mol) in diethyl ether (250 ml) is added a solution of tosyl chloride (225.7 g, 1.184 mol) in diethyl ether (800 ml) between −15° and −20° C. The resulting suspension is stirred at 0° C. for 1 hour, then 18 hours at ambient temperature. The reaction mixture is filtered, the solid residue is taken up twice in ethyl acetate and stirred, the suspension being filtered again. The combined ethyl acetate layers are evaporated to dryness giving a first crop of crude product (175.8 g). The ether filtrate is washed with water (2×) and brine, dried (Na2SO4), filtered, and partly concentrated. The suspension is filtered giving another 15.0 g of product. The crude solid product (190.8 g, 73%) is used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08084474B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-c9ed6bd26b3d48ca960346c188f758b7
출처 메모uspto-grants-2011_12