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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354364Generated: October 30, 2026

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

https://huagongshe.com/reaction/354364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzene, 1-isocyanato-2-methoxy-HCID 69695—
ReactantTert-butyl 4-amino-3-methylphenylacetateHCID 23512173—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 4-[N'-(2-methoxyphenyl)ureido]-3-methylphenylacetateHCID 2351252576.4%

Reaction Steps

To a stirred solution of tert-butyl 4-amino-3-methylphenylacetate (1.36 g, 6.15 mmol) and triethylamine (170 ml, 1.23 mmol) in THF (30 ml) was added 2-methoxyphenyl isocyanate (820 ml, 6.15 mmol), and the resulting mixture was stirred for 27 h. The mixture was concentrated to a small volume in vacuo, and hexane was added to the residue to give precipitate, which was collected by filtration to give tert-butyl 4-[N′-(2-methoxyphenyl)ureido]-3-methylphenylacetate (1.74 g, 76%) as a white crystallize material. mp 157-158° C.; 1H-NMR (CDCl3) δ1.46 (s, 9 H), 2.30 (s, 3 H), 3.50 (s, 2 H), 3.76 (s, 3 H), 6.43 (s, 1H), 6.83 (br d, J=8.4 Hz, 1 H), 6.95 (br d, J=8.0 Hz, 1 H), 6.98-4.99 (m, 2 H), 7.13 (brs, 1 H), 7.23 (br s, 1 H), 7.48 (d, J=8.8 Hz, 1 H), 8.14 (d, J=8.4 Hz, 1 H); MS (ESI) m/z 371 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756378B2
Source datasetuspto-grants-2004_06
ORD IDord-b2920a9081ba4e62add19c2f97cee011
Source noteuspto-grants-2004_06