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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410591Generated: October 25, 2026

Methanol → Methyl 3-{[2-(5-bromo-1,3-thiazol-2-yl)propan-2-yl]sulfonyl}propanoate

https://huagongshe.com/reaction/410591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMagnesium 2-(dioxidan-2-ide-1-carbonyl)benzoate--water (1/1/6)HCID 21894687—
ReactantMethyl 3-(2-(5-bromothiazol-2-yl)propan-2-ylthio)propanoateHCID 58456087—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium ThiosulfateHCID 24477—
ProductMethyl 3-{[2-(5-bromo-1,3-thiazol-2-yl)propan-2-yl]sulfonyl}propanoateHCID 6725809596%

Reaction Steps

The product of Step 3 (12.50 g, 38.5 mmol) was taken up in dichloromethane (250 mL)/methanol (125 mL), and magnesium monoperoxyphthalate hexahydrate (35.8 g, 57.8 mmol) was added. The reaction was stirred at room temperature for 2 h. The white slurry was diluted with 10% Na2S2O3 and water and extracted with CH2Cl2 (2×). The combined organic layers were washed with saturated NaHCO3, dried (MgSO4), filtered and evaporated. Flash chromatography (0-40% ethyl acetate in hexanes) afforded 13.12 g (96%) of methyl 3-{[2-(5-bromo-1,3-thiazol-2-yl)propan-2-yl]sulfonyl}propanoate as a white solid. ESI: [M+H]+ m/z 355.9/357.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-c7d37a4e5e6e448ba6d62a6474a12201
Source noteuspto-grants-2014_06