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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182646Generated: October 26, 2026

Tetrahydrofuran → Methacrylic acid 1-(1-ethylcyclopentyloxycarbonyl)-1,1-difluoro-2-butyl ester

https://huagongshe.com/reaction/1182646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-1-ethylcyclopentaneHCID 12859568—
Reactant2,2-Difluoro-3-(methacryloyloxy)pentanoic acidHCID 58413440—
SolventWaterHCID 962—
ProductMethacrylic acid 1-(1-ethylcyclopentyloxycarbonyl)-1,1-difluoro-2-butyl esterHCID 6668675983%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 2 L reactor was charged under nitrogen with 5.6 g (purity 78%, 20.0 mmol) of methacrylic acid 1-hydroxycarbonyl-1,1-difluoro-2-butyl ester and 240 mL of THF (dehydrated), followed by cooling down to 0° C., adding 5.2 mL (37.6 mmol/1.9 equivalents) of triethylamine, and stirring at 0° C. for 10 minutes. Then, furthermore 14.24 g (3.2 mmol/1.6 equivalents) of 1-chloro-1-ethylcyclopentane was added, followed by stirring at 0° C. for 20 minutes. To the reaction liquid 800 mL of water was added, followed by extraction two times with diisopropyl ether, removing water by magnesium sulfate, conducting a filtration, and distilling diisopropyl ether out, thereby obtaining 5.52 g of the target methacrylic acid 1-(1-ethylcyclopentyloxycarbonyl)-1,1-difluoro-2-butyl ester. Upon this, purity was 96%, and yield was 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08663903B2
Source datasetuspto-grants-2014_03
ORD IDord-096255fd802f46a29de630ec9c9026b9
Source noteuspto-grants-2014_03