Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296026Generated: October 31, 2026

Ethyl isocyanate → HCID 58909990, compound

https://huagongshe.com/reaction/1296026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanateHCID 8022—
ReactantTriethylamineHCID 8471—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
ReactantHCID 58910060HCID 58910060—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 58909990HCID 58909990—

Reaction Steps

Triethylamine (0.02 ml, 0.130 mmol) and ethyl isocyanate (0.053 ml, 0.677 ml) were added to a solution of 1-[3-(tert-butyl)-5-ethoxy-4-hydroxyphenyl]-1-ethanone (100 mg, 0.423 mmol) in methylene chloride (4.2 ml) and the mixture was stirred at room temperature for 2 days. Ethyl acetate was added, and then the reaction mixture was washed with water, the organic layer was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. Tetra-n-butylammonium tribromide (214 mg, 444 mmol) was added to a solution of the residue in methylene chloride-methanol (5 ml:1.2 ml) and the mixture was stirred at room temperature for 8 hours. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (142 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-834ac0f9174c4a7b891d6d7f3eb1f446
Source noteuspto-grants-2007_07