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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592720Generated: November 1, 2026

Isobutyl iodide → HCID 17952293, compound

https://huagongshe.com/reaction/1592720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl iodideHCID 10556—
ReactantPotassium CarbonateHCID 11430—
Reactant2-BromobenzenethiolHCID 80598—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 17952293HCID 17952293100%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 2-bromobenzene thiol (10.0 g, 52.8 mmol, 1.0 eq.) in DMF (250 mL) was added K2CO3 (17.5 g, 126.7 mmol, 2.4 eq.) and isobutyl iodide (7.3 mL, 63.36 mmol, 1.2 eq). The reaction was warmed to about 40° C. and stirred overnight. The mixture was diluted with EtOAc (300 mL) and washed with water (100 mL) and brine (100 mL). The organic layer was extracted with EtOAc(2×). The combined organic extracts were dried (Na2SO4), filtered and concentrated to afford 1-bromo-2-isobutylsulfanyl-benzene (12.94 g, 52.8 mmol, 100%), which is then taken to the next step without any further purification. GCMS (EI): 244.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291619B2
Source datasetuspto-grants-2007_11
ORD IDord-5b91ce23059349ed9d384ddca69787fe
Source noteuspto-grants-2007_11