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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272732Generated: October 25, 2026

4-Methyl-5-(2-hydroxyethyl)thiazole → 5-[2-(4-Bromo-2-methoxyphenoxy)ethyl]-4-methyl-1,3-thiazole

https://huagongshe.com/reaction/272732

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-5-(2-hydroxyethyl)thiazoleHCID 1136—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Bromo-2-methoxyphenolHCID 262234—
ReactantDibenzyl azodicarboxylateHCID 5387121—
SolventTetrahydrofuranHCID 8028—
Product5-[2-(4-Bromo-2-methoxyphenoxy)ethyl]-4-methyl-1,3-thiazoleHCID 69217389—

Reaction Steps

A mixture of 4-bromo-2-methoxy-phenol (50.8 mg, 0.25 mmol), 2-(4-methyl-thiazol-5-yl)-ethanol (49.5 mg, 0.25 mmol) and polymer-supported triphenyl phosphine (250 mg, 0.75 mmol) in THF (2.5 mL) was stirred at room temperature for 20 minutes. DBAD (86.3 mg, 0.375 mmol) was added and the mixture was stirred overnight at room temperature. The reaction mixture was filtered through Celite®, rinsing with THF and methanol. The filtrate was concentrated, diluted with ethyl acetate, washed with water and brine, dried (MgSO4), filtered and concentrated. The concentrate was purified by column chromatography on silica gel (10 to 20% ethyl acetate in hexane) to give the title compound. MS (ESI) m/e 329 (M+H)+; 1H NMR (300 MHz, DMSO-d6) □ 8.82 (s, 1H), 7.12 (d, J=2.4 Hz, 1H), 7.03 (dd, J=8.5, 2.4 Hz, 1H), 6.91 (d, J=8.5 Hz, 1H), 4.10 (t, J=6.4 Hz, 2H), 3.77 (s, 3H), 3.20 (t, J=6.4 Hz, 2H), 2.35 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456169B2
Source datasetuspto-grants-2008_11
ORD IDord-ed514b5f95dd4b72bf78e549e5649397
Source noteuspto-grants-2008_11