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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198276Generated: November 2, 2026

Hydrochloric Acid → 1-(4-Methyl-2-thiazolyl)-2-(2-chloroethoxy)ethanol

https://huagongshe.com/reaction/1198276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Methyl-1,3-thiazole-2-carbaldehydeHCID 4263432—
ReactantHCID 178478511HCID 178478511—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(4-Methyl-2-thiazolyl)-2-(2-chloroethoxy)ethanolHCID 53850153—

Reaction Conditions

Temperature-30 °C

Reaction Steps

1.6 g of 4-methyl-2-formylthiazole was dissolved in 30 ml of tetrahydrofuran. The solution was cooled to -30° C. Thereto was dropwise added, in 10 minutes, 10 ml of a tetrahydrofuran solution containing 1.6M of 2-chloroethoxymethylmagnesium chloride. The mixture was stirred for 1 hour with ice cooling. The reaction mixture was added to a mixture of 50 ml of ice water, 50 ml of ethyl acetate and 2 g of ammonium chloride. The resulting mixture was adjusted to pH 2 with 6N hydrochloric acid and stirred at the same temperature for 5 minutes. The reaction mixture was adjusted to pH 6 with a saturated aqueous sodium hydrogencarbonate solution. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by column chromatography (eluant: toluene/ethyl acetate=4/1) to obtain 1.3 g of oily 1-(4-methyl-2-thiazolyl)-2-(2-chloroethoxy)ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05280032
Source datasetuspto-grants-1994_01
ORD IDord-d5855472080c4d82849060da602f7091
Source noteuspto-grants-1994_01