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HRID 2060936作成日:2026年10月27日

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

https://huagongshe.com/reaction/2060936

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-nitro-1,3-propanediolHCID 6480—
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物TriethylamineHCID 8471—
溶媒Diethyl EtherHCID 3283—
生成物2-Methyl-2-nitro-1,3-propanediol-di-p-toluenesulfonateHCID 5195535.7%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08278464B2
出典データセットuspto-grants-2012_10
ORD IDord-32974668cc244d5bbec78c16528d8615
出典メモuspto-grants-2012_10