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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593719Generated: October 26, 2026

Butyl methanesulfonate → Butyl Stearate

https://huagongshe.com/reaction/1593719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl methanesulfonateHCID 15953—
ReactantButyl StearateHCID 31278—
ReactantPotassium StearateHCID 23673840—
ProductButyl StearateHCID 31278—
ProductPotassium methanesulphonateHCID 23666501—

Reaction Steps

An esterification reaction mixture (94 g), consisting of butanol (ca., 4.9% w/w), butyl stearate (95.1% w/w), residual stearic acid (trace), residual methanesulfonic acid catalyst (1383 ppm) and undesired butyl methanesulfonate (613 ppm) was treated with 45% aqueous KOH (229 mg, 1.84 mmol as compared to 1.74 mmol MSA originally charged to the reaction). The resulting mixture was heating at 50° C. for 40 minutes. Without wishing to be bound by any particular theory or explanation, it is believed that reaction of butyl stearate with KOH produced potassium stearate, which retains significant solubility in the butyl stearate medium. The formed potassium stearate then reacted with butyl methanesulfonate to produce potassium methanesulfonate and butyl stearate. After filtration of the by-product solid salts (0.6325 g), analysis of the mixture by gas chromatography revealed only 300 ppm unreacted butyl methanesulfonate, a 51% reduction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297813B2
Source datasetuspto-grants-2007_11
ORD IDord-10d5384285bd45ec8ec72b7fe6287bbb
Source noteuspto-grants-2007_11