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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625083Generated: November 1, 2026

Hydrochloric Acid → Ethyl 2-bromo-2-(4-methyl-1,3-thiazol-2-yl)propanoate

https://huagongshe.com/reaction/1625083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium BromideHCID 253877—
ReactantEthyl 2-(4-methyl-1,3-thiazol-2-yl)propanoateHCID 66751996—
SolventTolueneHCID 1140—
ProductEthyl 2-bromo-2-(4-methyl-1,3-thiazol-2-yl)propanoateHCID 6675171397%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of Intermediate 104 (7.57 g, 38.0 mmol) in toluene (100 mL) was added hydrochloric acid (3.43 mL, 41.8 mmol). The mixture was kept at room temperature for 10 minutes. The mixture was cooled to 0° C. and potassium bromide (PANREAC, 4.97 g, 41.8 mmol) and hydrogen peroxide (4.59 mL, 49.4 mmol) were added. Reaction mixture was stirred at 0° C. for 3 hours and then was quenched with 1N Na2S2O3 (150 mL) and saturated NaHCO3 aqueous solution (150 mL). Organic phase was separated and the aqueous phase was extracted with EtOAc (2×150 mL). Combined organic layers were washed with brine, dried over sodium sulfate and concentrated to give the title compound (10.22 g, 36.7 mmol, 97% yield) as oil. 1H NMR (300 MHz, DMSO-d6) δ ppm: 7.43 (m, 1H), 4.21-4.28 (q, 2H), 2.30-2.35 (m, 6H), 1.19-1.24 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779153B2
Source datasetuspto-grants-2014_07
ORD IDord-f89b48f366ec4ac7a4b253cce9cea280
Source noteuspto-grants-2014_07