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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422555Generated: November 1, 2026

Methyl iodide → (4-Bromo-3-methylphenyl)(methyl)sulfane

https://huagongshe.com/reaction/422555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-3-methylbenzene-1-thiolHCID 15661105—
SolventDimethylformamideHCID 6228—
Product(4-Bromo-3-methylphenyl)(methyl)sulfaneHCID 2637018999.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-bromo-3-methylbenzenethiol (5.47 g, 26.9 mmol) in DMF (25 mL) was added NaH (0.743 g, 32.3 mmol) at RT. After 15 minutes at RT, the solution was cooled to 0° C. and iodomethane (2.02 ml, 32.3 mmol) was added. The cooling bath was removed and the mixture was allowed to warm up to RT. After 1 hour, water was added and the mixture was extracted with EtOAc (3×). The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated to give 5.81 g of (4-bromo-3-methylphenyl)(methyl)sulfane as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101612B2
Source datasetuspto-grants-2012_01
ORD IDord-681b44b80a914c4ea9a700a725aa2305
Source noteuspto-grants-2012_01