HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → HCID 46199367, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Ethyl 3-(3-(4-octylphenyl)ureido)propanoate | HCID 66615004 | — |
| Product | HCID 46199367 | HCID 46199367 | 65.5% |
Reaction Steps
To a solution of the product of Step A (0.05 g; 0.143 mmol) in dioxane (1 ml) 2N KOH (0.36 ml; 0.72 mmol) was added and the mixture was refluxed for 15 min, cooled to room temperature and evaporated to dryness under reduced pressure. The residue was diluted to 2 ml with H2O and filtered. The filtrate was acidified to pH ˜4 with citric acid. The solid formed was filtered off, washed with H2O (3×2 ml), dried in vacuo to give the title compound (0.03 g; 65%), as a colourless solid. 1H-NMR (CD3OD+CDCl3) 7.16 (d, 2H, J=8.4 Hz); 7.0 (d, 2H, J=8.4 Hz); 4.21 (s, CD3OH); 3.4 (t, 2H, J=6.7 Hz); 2.73 (m, 4H); 2.5-2.44 (m, 4H); 1.5 (m, 2H); 1.2 (m, 10H); 0.81 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193716B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-1956ca2cf9e64806bceeadd03ba1f5de |
| Source note | uspto-grants-2015_11 |