HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenoxyphenyl isocyanate → 1-Hydroxy-1-(1-ethylpropyl)-3-(4-phenoxyphenyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenoxyphenyl isocyanate | HCID 2734896 | — |
| Reactant | N-(pentan-3-yl)hydroxylamine | HCID 19073513 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Hydroxy-1-(1-ethylpropyl)-3-(4-phenoxyphenyl)urea | HCID 19967381 | 50.9% |
Reaction Steps
A solution of N-(1-ethylpropyl)hydroxylamine (1.13 g, 11 mmole, Compound 39, Part B) in tetrahydrofuran (30 mL) was charged with 4-phenoxyphenylisocyanate (2.1 g, 10 mmole) and maintained at ambient temperature overnight. The solvent was removed in vacuo to yield 3.2 g of the crude product as a white solid. Recrystallization from hexanesethyl acetate provided 1.6 g of the desired product as a white crystalline solid, m.p. 124°-125° C. Analysis: Calculated for: C18H22N2O3 : %C, 68.77; %H, 7.05; %N, 8.91; Found: %C, 68.44; %H, 7.09; %N, 8.82.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05612377 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-0172f93dfd3b4ccfb0abf7fa379994cc |
| Source note | uspto-grants-1997_03 |