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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414654Generated: October 25, 2026

Pyridine → Ethyl 2-(2-bromopropionyloxy)-ethylcarbamate

https://huagongshe.com/reaction/414654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPropanoyl bromide, 2-bromo-HCID 79047—
Reactantethyl N-(2-hydroxyethyl)carbamateHCID 223805—
SolventDiethyl EtherHCID 3283—
ProductEthyl 2-(2-bromopropionyloxy)-ethylcarbamateHCID 54505068—

Reaction Steps

A solution of 32.4 g of 2-bromopropionyl bromide in 70 ml of diethyl ether is added dropwise within one hour while cooling with ice to a solution, cooled to 0° C., of ethyl 2-hyroxyethylcarbamate and 13.1 g of pyridine in 80 ml of diethyl ether. The reaction mixture is then stirred at room temperature for 45 minutes. For the working-up, the mxture is filtered under suction through Celite and the filtrate is poured into water. The aqeuous phase is extracted twice with diethyl ether, and the combined organic phases are washed twice with water and once with saturated sodium chloride solution, dried over anhydrous sodium sulphate and evaporated to dryness. There is obtained ethyl 2-(2-bromopropionyloxy)-ethylcarbamate as a colourless oil which either can be used in the reaction without further purification or can be purified further by chromatography on silica gel with n-hexane/diethyl ether (1:1); nD20 1.4770.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792616
Source datasetuspto-grants-1988_12
ORD IDord-11d59787ad1145b99cf336fae887135a
Source noteuspto-grants-1988_12