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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375194Generated: November 2, 2026

Methyl iodide → HCID 10380418, compound

https://huagongshe.com/reaction/1375194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10039936HCID 10039936—
SolventDimethylformamideHCID 6228—
ProductHCID 10380418HCID 1038041868%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-chloro-N-[(1S,2S)-1-(hydroxymethyl)-2-methylbutyl]benzenesulfonamide (0.10 g, 0.343 mmol) dissolved in DMF (2.0 mL) was added potassium carbonate (47 mg, 0.343 mmol). After 30 minutes, the reaction mixture was cooled to 0° C. and iodomethane (50 μL, 0.686 mmol) was added. After 2 hours, the ice bath was removed and the reaction mixture was stirred at 25° C. for 24 hours. The insolubles were then filtered off and the DMF solution was diluted with EtOAc (50 mL) and washed sequentially with 10% citric acid (50 mL) and saturated brine (50 mL), dried over MgSO4 and evaporated to a clear oil which was washed with Et2O and then purified by flash chromatography (eluant: 95-5 CHCl3/iPrOH) to afford the desired product as a clear oil (71 mg, 68%). Mass Spectrum (+APCI): 306 ([M+H]+). Anal: Calc'd for C13H20ClNO3S: C, 51.06; H, 6.59; N, 4.58. Found: C, 51.15; H, 6.73; N, 4.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166622B2
Source datasetuspto-grants-2007_01
ORD IDord-030d8daf21494ff49cdb45e107873a2a
Source noteuspto-grants-2007_01