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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156216Generated: November 2, 2026

Tetrahydrofuran → Ethylthioethyl-2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoate

https://huagongshe.com/reaction/1156216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoyl chlorideHCID 12799632—
ReactantEthylthioethanolHCID 19024902—
ProductEthylthioethyl-2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoateHCID 1279964653%

Reaction Steps

In 20 ml tetrahydrofuran were dissolved 0.8 g (0.0075 mol) of ethyl thioethanol and 0.8 g (0.0079 mol) of triethylamine, and while heating to 60°-80° C., 1.6 g (0.0043 mol) of 2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoyl chloride was added. After 5-hour stirring, the resulting mixture was cooled, freed of the solvent under reduced pressure, and extracted with benzene. The extract was washed with a dilute aqueous solution of caustic soda and then with dilute hydrochloric acid, and dehydrated with sodiumsulfate. By concentration, 1.0 g (0.0023 mol) of the intended product was obtained as an oily substance; yield 53.0%, nD23 1.5500.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04334914
Source datasetuspto-grants-1982_06
ORD IDord-1050a243f08c4fdc88ebd265f0040270
Source noteuspto-grants-1982_06