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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041986Generated: October 30, 2026

Ethyl isocyanate → HCID 59577314, compound

https://huagongshe.com/reaction/2041986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanateHCID 8022—
Reactant3-(2-Tert-butylphenoxy)azetidineHCID 53409530—
SolventPyridineHCID 1049—
ProductHCID 59577314HCID 5957731453.2%

Reaction Steps

To a stirred solution of 3-(2-tert-Butylphenoxy)azetidine (0.21 g, 1.02 mmol) in pyridine (10 ml) was added ethyl isocyanate (0.078 g, 1.10 mmol) and the mixture was stirred at room temperature for 16 h. The reaction mixture was concentrated under reduced pressure and the resulting residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was washed with water and saturated sodium chloride, dried (MgSO4), filtered and concentrated under reduced pressure. The resulting residue was triturated with heptane/ethyl acetate to provide 3-(2-tert-Butylphenoxy)-N-ethylazetidine-1-carboxamide (0.15 g, 53%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586571B2
Source datasetuspto-grants-2013_11
ORD IDord-c83e5fb0c7544e12acc598e28a15097b
Source noteuspto-grants-2013_11