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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226194Generated: October 26, 2026

Iodoethane → Ethyl 2-[2-chloro-4-(3,5-difluorophenoxy)phenoxy]ethylthiocarbamate

https://huagongshe.com/reaction/2226194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantTriethylamineHCID 8471—
ReactantCarbonyl SulfideHCID 10039—
Reactant2-[2-Chloro-4-(3,5-difluorophenoxy)phenoxy]ethylamineHCID 15766489—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-[2-chloro-4-(3,5-difluorophenoxy)phenoxy]ethylthiocarbamateHCID 5383571861%

Reaction Steps

Into a mixture of 1.20 g of 2-[2-chloro-4-(3,5difluorophenoxy)phenoxy]ethylamine, 0.81 g of triethylamine and 20 ml of tetrahydrofuran, excesss of carbonyl sulfide gas was introduced with stirring at room temperature for 30 minutes. To the above mixture, there was added dropwise 0.75 g of ethyl iodide, and the resultant mixture was stirred at the same temperature for 24 hours. The reaction mixture was concentrated, and the residue was poured into 100 ml of water and extracted twice with 100 ml of ethyl acetate. The extracts were combined together, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography to give 0.95 g of ethyl 2-[2-chloro-4-(3,5-difluorophenoxy)phenoxy]ethylthiocarbamate. Yield: 61%. nD21 : 1.5707.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05346920
Source datasetuspto-grants-1994_09
ORD IDord-b79b53482b844b0eadbbb594662579ea
Source noteuspto-grants-1994_09