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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047953Generated: November 2, 2026

Chloromethyl Methyl Ether → 1-(Methoxymethyl)oxycarbonyl-1,1-difluoro-2-butyl methacrylate

https://huagongshe.com/reaction/2047953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantTetrahydrofuranHCID 8028—
Reactant2,2-Difluoro-3-(methacryloyloxy)pentanoic acidHCID 58413440—
SolventWaterHCID 962—
Product1-(Methoxymethyl)oxycarbonyl-1,1-difluoro-2-butyl methacrylateHCID 5986383283%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under nitrogen, a 20 mL reactor was charged with 70 mg (0.25 mmol) of 1-hydroxycarbonyl-1,1-difluoro-2-butyl methacrylate (purity: 78%) and 3 mL of THF (dehydrated one), followed by cooling to 0° C. Then, 65 μL (0.47 mmol, 1.9 eq) was added, followed by stirring at 0° C. for 10 min. Then, 30 μL (0.40 mmol, 1.6 eq) of chloromethyl methyl ether was added, followed by stirring at 0° C. for 20 min. Then, 5 mL of water was added to the reaction solution, followed by extraction with diisopropyl ether two times and removal of water with magnesium sulfate. After conducting filtration, diisopropyl ether was distilled off, thereby obtaining 58 mg of the target 1-(methoxymethyl)oxycarbonyl-1,1-difluoro-2-butyl methacrylate. Upon this, purity was 96%, and yield was 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592622B2
Source datasetuspto-grants-2013_11
ORD IDord-b0b8664efa1940e492a87844a9c86306
Source noteuspto-grants-2013_11