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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657512Generated: October 27, 2026

Methanol → Methyl 2-acrylamido-2-methylpropanesulfonate

https://huagongshe.com/reaction/1657512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcrylonitrileHCID 7855—
ReactantIsobutyleneHCID 8255—
Reactant4-MethoxyphenolHCID 9015—
ReactantFuming sulfuric acidHCID 24681—
ProductMethyl 2-acrylamido-2-methylpropanesulfonateHCID 19088270—

Reaction Steps

Following substantially the procedure of Example 1, a reaction mixture is prepared from 400.3 grams (4.45 gramatoms of sulfur) of 40% oleum, 1930 grams (36.4 moles) of acrylonitrile (containing 0.013% water) and 56 grams (1 equivalent) of isobutene. The addition rates are the same as in Example 1 except that the oleum addition rate is 6.8 grams per minute. Following the completion of the acrylonitrile and isobutene addition, oleum addition is continued until the indicated amount has been introduced. The reaction mixture is then poured into 128 grams (4 moles) of methanol at 5°-10°C., over one hour. p-Methoxyphenol, 0.5 gram, is added as a polymerization inhibitor and the solution is poured over 1000 grams of ice. The organic layer is separated; the aqueous layer is washed with aqueous sodium sulfate solution and extracted with three 500-ml. portions of chloroform. The organic layer and chloroform extracts are dried over magnesium sulfate and the volatile materials are stripped to yield the desired methyl 2-acrylamido-2-methylpropanesulfonate which is recrystallized from a benzene-cyclohexane mixture. The recrystallized product melts at 78°-81°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03960918
Source datasetuspto-grants-1976_06
ORD IDord-a4ae0d621a3a4030b0d3074854d34e6a
Source noteuspto-grants-1976_06