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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354371Generated: October 26, 2026

Triethylamine → tert-butyl 4-[N'-(2,6-dichlorophenyl)ureido]-3-methylphenylacetate

https://huagongshe.com/reaction/354371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-Dichloro-2-isocyanatobenzeneHCID 604537—
ReactantTert-butyl 4-amino-3-methylphenylacetateHCID 23512173—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 4-[N'-(2,6-dichlorophenyl)ureido]-3-methylphenylacetateHCID 2351235174.1%

Reaction Steps

To a mixture of tert-butyl 4-amino-3-methylphenylacetate (1.88 g, 8.51 mmol), 2,6-dichlorophenyl isocyanate (1.60 g, 8.51 mmol) in THF (40 ml) was added Et3N (0.24 ml, 1.70 mmol) at room temperature. After 3 h stirring, the reaction mixture was concentrated in vacuo. The residue was triturated by the addition of n-hexane, to give tert-butyl 4-[N′-(2,6-dichlorophenyl)ureido]-3-methylphenylacetate (2.58 g, 74%) as a colorless powder. mp 243-244° C. (dec.); 1H-NMR (CDCl3) δ1.45 (s, 9H), 2.30 (s, 3H), 3.49 (s, 2H), 6.24 (s, 2H), 7.12-7.16 (m, 3H), 7.35 (d, J=8.3 Hz, 2H), 7.51 (d, J 7.8H, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756378B2
Source datasetuspto-grants-2004_06
ORD IDord-1189e5d8c2ab404ba698615b5c8aeaca
Source noteuspto-grants-2004_06