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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360534Generated: November 4, 2026

1-Butanol → Methacrylic acid 1-(n-butoxycarbonyl)-1,1-difluoro-2-butyl ester

https://huagongshe.com/reaction/2360534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantDiisopropyl EtherHCID 7914—
ReactantTriethylamineHCID 8471—
ReactantMethacrylic acid 1-chlorocarbonyl-1,1-difluoro-2-butyl esterHCID 58352381—
ProductMethacrylic acid 1-(n-butoxycarbonyl)-1,1-difluoro-2-butyl esterHCID 8666348991.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 1 L glass flask with a dropping funnel, 62.8 g (0.847 mol, 1.2 eq) of n-butanol, 510 g of diisopropyl ether, 100 g (0.988 mol, 1.4 eq) of triethylamine and 1 g of antioxidant “Nonflex MBP” (manufactured by Seiko Chemical Co., Ltd.) were added. The resulting solution was cooled to 0° C. and stirred, followed by dropping thereto 170 g (purity: 99%, 0.706 mol) of methacrylic acid 1-chlorocarbonyl-1,1-difluoro-2-butyl ester. The thus-obtained reaction solution was stirred for 1 hour at room temperature. The completion of the reaction was confirmed by 19F NMR. The reaction-completed solution was separated into an organic layer and an aqueous layer by the addition of 500 mL of water. The organic layer was dehydrated with magnesium sulfate, filtrated, and then, concentrated under a reduced pressure. The concentration residue was subjected to distillation under a reduced pressure. With this, 179 g of methacrylic acid 1-(n-butoxycarbonyl)-1,1-difluoro-2-butyl ester was obtained as a colorless transparent liquid (yield: 91%, purity: 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686098B2
Source datasetuspto-grants-2014_04
ORD IDord-61770f73d3f64fcdbd3f75849c83f717
Source noteuspto-grants-2014_04