HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38679Generated: October 28, 2026
Hydrochloric Acid → Ethyl 2-bromo-2-(4-methyl-1,3-thiazol-2-yl)propanoate
https://huagongshe.com/reaction/38679
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | Ethyl 2-(4-methyl-1,3-thiazol-2-yl)propanoate | HCID 66751996 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-bromo-2-(4-methyl-1,3-thiazol-2-yl)propanoate | HCID 66751713 | 92% |
Reaction Steps
To a solution of ethyl 2-(4-methyl-1,3-thiazol-2-yl)propanoate (3.91 g, 19.62 mmol) in toluene (95 mL) was added hydrochloric acid (1.77 mL, 21.58 mmol). The mixture was stirred at room temperature for 10 minutes. The mixture was cooled to 0° C. and then potassium bromide (MERCK, 2.57 g, 21.58 mmol) and hydrogen peroxide (2.37 mL, 25.5 mmol) were added. Reaction mixture was stirred at 0° C. for 5 hours, at which point TLC (1:1 EtOAc-Hex) showed reaction had gone to completion. Reaction mixture was quenched with 1N Na2S2O3 (60 mL) and saturated NaHCO3 (60 mL). Organic phase was separated and the aqueous phase was extracted with ethyl acetate (2×60 mL). Combined organics were washed with brine, dried over sodium sulfate and concentrated to give the title compound (5.02 g, 18.05 mmol, 92% yield) as a red oil. 1H-NMR (300 MHz, DMSO-d6) δ ppm: 7.41 (s, 1H), 4.23 (q, 3H), 2.33 (s, 3H), 2.28 (s, 3H), 1.20 (t, 3H). [ES+MS] m/z 278 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524750B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-48522d978d164c8a9261f86f9035c50c |
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| Source note | uspto-grants-2013_09 |
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