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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660123Generated: October 26, 2026

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

https://huagongshe.com/reaction/660123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-nitro-1,3-propanediolHCID 6480—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
SolventDiethyl EtherHCID 3283—
Product2-Methyl-2-nitro-1,3-propanediol-di-p-toluenesulfonateHCID 5195535.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084474B2
Source datasetuspto-grants-2011_12
ORD IDord-c9ed6bd26b3d48ca960346c188f758b7
Source noteuspto-grants-2011_12