HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 14208609, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 14208608 | HCID 14208608 | — |
| Product | HCID 14208609 | HCID 14208609 | — |
Reaction Steps
A mixture of the product from Example 2 (0.30 g, 1.17 mole) and N-(4,6-dimethylpyrimidin-2-yl)phenyl carbamate (0.30 g, 1.23 mmole) in acetonitrile (30 mL) was treated with DBU (184 μl, 1.23 mmole) at room temperature overnight. The solution was poured into water and acidified with acetic acid. The solid which precipitated was collected on a glass funnel and washed with water, butylchloride, and ether to yield 0.15 g white solid; m.p. 190°-192° C.; NMR (CDCl3)δ: 2.0-2.2 (m, 2H), 2.3-2.5 (m, with s at δ2.44, 8H), 2.7-2.8 (m, 2H), 6.25 (s, 1H), 6.77 (s, 1H), 7.36 and 7.66 (AB q, J=5.4 Hz, 2H); IR cm-1 (nujol): 1730, 1700 (shoulder at 1685 and 1675), 1605, 1550, 1170, 1140.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04756742 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-fd085077e8894d878e441318e60bb599 |
| Source note | uspto-grants-1988_07 |