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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253347Generated: October 26, 2026

2-Chloro-1,1,1-triethoxyethane → 2-(Chloromethyl)-5-(trifluoromethyl)-1,3-benzothiazole

https://huagongshe.com/reaction/1253347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,1,1-triethoxyethaneHCID 305922—
Reactant2-Amino-4-(trifluoromethyl)benzenethiol hydrochlorideHCID 2734678—
SolventEthanolHCID 702—
Product2-(Chloromethyl)-5-(trifluoromethyl)-1,3-benzothiazoleHCID 14204205—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2-amino-4-trifluoromethylthiophenol hydrochloride (30.0 g) in ethanol (125 ml) was added 2-chloro-1,1,1-triethoxyethane (31.0 g). The mixture was heated for 1 hour at 60° C. The solution was concentrated to remove excess ethanol and the resulting material was extracted with ether (500 ml). The organic extract was washed successively with 10% HCl (20 ml), water (100 ml), 10% sodium bicarbonate solution and water (100 ml), and then evaporated to obtain an amber colored oil, which crystallized upon standing at room temperature (28.9 g; m.p. 52° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748280
Source datasetuspto-grants-1988_05
ORD IDord-a0e26934030546cf9b0f1d6dc0610931
Source noteuspto-grants-1988_05