HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl isocyanate → tert-butyl 3-methyl4-(N'-phenylureido)phenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-butyl 4-amino-3-methylphenylacetate | HCID 23512173 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl 3-methyl4-(N'-phenylureido)phenylacetate | HCID 23512058 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179819B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-ad443521b9454dc1ab410e655171c012 |
| Source note | uspto-grants-2007_02 |