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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549666Generated: October 29, 2026

Methyl iodide → 6-Chloro-2-(methylsulfinyl)benzo[d]oxazole

https://huagongshe.com/reaction/549666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-Chlorobenzoxazole-2(3H)-thioneHCID 2119214—
SolventTetrahydrofuranHCID 8028—
Product6-Chloro-2-(methylsulfinyl)benzo[d]oxazoleHCID 59671466—

Reaction Steps

Iodomethane (1.35 mL, 21.6 mmol) was added to a mixture of 6-chlorobenzo[d]oxazole-2(3H)-thione (2.00 g, 10.8 mmol) and K2CO3 (2.99 g, 21.6 mmol) in THF (43 mL). After 2 h, the reaction mixture was filtered and concentrated under reduced pressure. The crude material was dissolved in CH2Cl2 (40 mL) and meta-chloroperbenzoic acid (50-55%, 3.73 g, 10.8 mmol) was added at 0° C. The reaction was allowed to warm to rt. After stirring overnight, the reaction mixture was diluted with sodium thiosulfate (saturated, aqueous) and the organics were separated. The organics were washed with NaHCO3 (saturated, aqueous, 50 mL) and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. This gave 3.22 g (>100% crude yield) of the desired product as an orange solid. The material was used without further purification. LC-MS: RT=6.57 min., [M+H]+=216.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943622B2
Source datasetuspto-grants-2011_05
ORD IDord-7d659fcc78044ce987ba1347a86e832a
Source noteuspto-grants-2011_05