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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460995Generated: October 25, 2026

2-Bromo-1,1-dimethoxyethane → 2-(4-(Trifluoromethyl)phenyl)thiazole

https://huagongshe.com/reaction/1460995

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
Reactant4-(Trifluoromethyl)thiobenzamideHCID 2734823—
CatalystHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product2-(4-(Trifluoromethyl)phenyl)thiazoleHCID 1460196960%

Reaction Steps

A stirred solution of 5.0 grams (0.024 mole) of 4-trifluoromethylbenzthioamide, 4.4 grams (0.026 mole) of bromoacetaldehyde dimethyl acetal, and 4 drops of concentrated hydrochloric acid in 50 ml of ethanol was heated at reflux for 18 hours. After this time the reaction mixture was subjected to column chromatography on silica gel. Elution was accomplished using 20% ethyl acetate in hexane. The appropriate fractions were combined and concentrated under reduced pressure, yielding 3.3 grams of 2-(4-trifluoromethylphenyl)thiazole. The nmr spectrum was consistent with the proposed structure. The reaction was repeated several times.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05073564
Source datasetuspto-grants-1991_12
ORD IDord-52935fdb1b064cff904a505076b8fd46
Source noteuspto-grants-1991_12