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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350413Generated: October 26, 2026

Phenyl isocyanate → tert-butyl 3-methyl4-(N'-phenylureido)phenylacetate

https://huagongshe.com/reaction/350413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 4-amino-3-methylphenylacetateHCID 23512173—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 3-methyl4-(N'-phenylureido)phenylacetateHCID 2351205861%

Reaction Steps

To a stirred solution of tert-butyl 4-amino-3-methylphenylacetate (1.20 g, 5.42 mmol) and Et3N (830 ml, 5.95 mmol) in THF (10 ml) was added phenyl isocyanate (650 ml, 5.98 mmol) and the reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated to a small volume and diluted with n-hexane. Resulting precipitate was collected under a reduced pressure and the filtrate was washed with n-hexane to give tert-butyl 3-methyl4-(N′-phenylureido)phenylacetate (1.12 g, 61%) as a white crystalline powder. mp 143–145° C.; 1H-NMR (CDCl3) δ 1.47 (s, 9 H), 2.09 (s, 3 H), 3.47 (s, 2 H), 6.44 (s, 1 H), 7.01–7.07 (m, 4 H), 7.16–7.27 (m, 2 H), 7.30–7.33 (m, 2 H), 7.45–7.47 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-ad443521b9454dc1ab410e655171c012
Source noteuspto-grants-2007_02