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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393529Generated: October 27, 2026

Methyl iodide → 5-Bromo-2-(methylthio)benzo[d]oxazole

https://huagongshe.com/reaction/393529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-1,3-benzoxazole-2-thiolHCID 10633197—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Bromo-2-(methylthio)benzo[d]oxazoleHCID 2249579296%

Reaction Steps

5-Bromo-3H-benzooxazole-2-thione (530 mg, 2.30 mmol) was dissolved in DMF (5.75 mL). Potassium carbonate (318 mg, 2.30 mmol) and iodomethane (172 μL, 2.76 mmol) were added and the reaction mixture was allowed to stir at RT for 3.5 h. The mixture was diluted with water (10 mL) and extracted with ethyl acetate (4×10 mL). The combined organic extracts were washed with water (3×10 mL), brine (10 mL) and dried (Na2SO4), filtered and concentrated to afford 538 mg (96%) of the title compound as a dark brown solid: 1H NMR (CDCl3, 400 MHz) δ 7.72 (d, 1H, J=2.1 Hz), 7.36-7.26 (m, 2H), 2.75 (s, 3H); 13C NMR (CDCl3, 100 MHz) δ 167.6, 151.2, 143.8, 126.9, 121.6, 117.3, 111.2, 14.8; MS (Cl) m/z 244.0 (M+1); HPLC retention time=5.10 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809094B2
Source datasetuspto-grants-2004_10
ORD IDord-4094774b9401413c9f749b4e2ecb3f69
Source noteuspto-grants-2004_10