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HRID 1593719作成日:2026年10月27日

Butyl methanesulfonate → Butyl Stearate

https://huagongshe.com/reaction/1593719

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl methanesulfonateHCID 15953—
反応物Butyl StearateHCID 31278—
反応物Potassium StearateHCID 23673840—
生成物Butyl StearateHCID 31278—
生成物Potassium mesylateHCID 23666501—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07297813B2
出典データセットuspto-grants-2007_11
ORD IDord-10d5384285bd45ec8ec72b7fe6287bbb
出典メモuspto-grants-2007_11