Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669813Generated: October 28, 2026

Nitroethane → HCID 57438911, compound

https://huagongshe.com/reaction/1669813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitroethaneHCID 6587—
ReactantPhenyl isocyanateHCID 7672—
ReactantTriethylamineHCID 8471—
Reactant4-tert-ButylphenylacetyleneHCID 2757302—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 57438911HCID 57438911—

Reaction Steps

4.57 ml (42.12 mmol) of phenyl isocyanate are added dropwise at room temperature to a solution of 5 g (31.59 mmol) of 1-ethynyl-4-(tert-butyl)benzene, 0.75 ml (10.53 mmol) of nitroethane and 0.29 ml (2.10 mmol) of triethylamine in 100 ml of benzene. The reaction mixture is then stirred under reflux for 12 h. After cooling, the suspension is mixed with water (50 ml) and stirred at room temperature for a further 4 h. The precipitate is filtered off with suction and washed with benzene (10 ml). The organic phase of the filtrate is separated off, dried with magnesium sulfate and concentrated. The residue is purified by column chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 9:1). 989 mg (14% of theory) of the title compound are obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989633B2
Source datasetuspto-grants-2011_08
ORD IDord-79c17ad90d444752a46ffa740914ea99
Source noteuspto-grants-2011_08