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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975758Generated: October 31, 2026

Methyl iodide → HCID 10836157, compound

https://huagongshe.com/reaction/1975758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 9844519HCID 9844519—
SolventAcetonitrileHCID 6342—
ProductHCID 10836157HCID 10836157—

Reaction Steps

1,8-Diazabicyclo[5.4.0]undec-7-ene (1.6 mL, 10.7 mmol) was added dropwise to a solution of N-[2,6-bis(1-methylethyl)phenyl]-N'-[(dibutylamino)sulfonyl]urea (4.0 g, 9.7 mmol) and methyl iodide (1.52 g, 10.7 mmol) in 100 mL acetonitrile at -15° C. The resulting mixture was warmed to room temperature and stirred for 16 hours. Concentrated in vacuo and partitioned between 1N HCl and ethyl acetate. The organic layer was dried with MgSO4, filtered, and concentrated to give an orange oil. Chromatography gave the title compound as a clear oil; 1H NMR (DMSO-d6) θ 8.57 (s, 1H), 7.31-7.15 (m, 3H), 3.33-3.21 (m, 7H), 3.05 (heptet, 2H), 1.57-1.46 (m, 4H), 1.35-1.20 (m, 4H), 1.13 (d, 12H), 0.90 (t, 6H). ##STR14##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288757
Source datasetuspto-grants-1994_02
ORD IDord-9546d98f73794d42982aa37e257246d3
Source noteuspto-grants-1994_02