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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363909Generated: October 26, 2026

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

https://huagongshe.com/reaction/1363909

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 numberUS07887990B2
Source datasetuspto-grants-2011_02
ORD IDord-edd60f31e4f040608c955d04a4b62784
Source noteuspto-grants-2011_02