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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506736Generated: October 27, 2026

Triethylamine → 2-Ethoxycarbonyl-2,2-difluoro-1-phenylethyl 1-adamantanecarboxylate

https://huagongshe.com/reaction/1506736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Adamantanecarbonyl chlorideHCID 98915—
ReactantEthyl 2,2-difluoro-3-hydroxy-3-phenylpropanoateHCID 11138943—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-Ethoxycarbonyl-2,2-difluoro-1-phenylethyl 1-adamantanecarboxylateHCID 11796669297.8%

Reaction Steps

In 60 g of methylene chloride were dissolved 9 g of ethyl 2,2-difluoro-3-hydroxy-3-phenylpropionate, prepared in Synthesis Example 1-4, and 9.5 g of 1-adamantanecarbonyl chloride. Under ice cooling, a mixture of 6 g of triethylamine, 0.5 g of 4-dimethylaminopyridine and 20 g of methylene chloride was added dropwise to the solution. The reaction solution was aged overnight, after which it was quenched with 5 wt % hydrochloric acid, washed with water, and concentrated. Methyl isobutyl ketone was added to the concentrate, which was concentrated again. There was obtained 15 g of the target compound, 2-ethoxycarbonyl-2,2-difluoro-1-phenylethyl 1-adamantanecarboxylate as colorless oily matter (yield 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221742B2
Source datasetuspto-grants-2015_12
ORD IDord-a4d8b01fb6954133a2afec85748c072e
Source noteuspto-grants-2015_12