HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505903Generated: October 31, 2026
Carbamic acid, ethyl-, ethyl ester → HCID 58266356, compound
https://huagongshe.com/reaction/1505903
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbamic acid, ethyl-, ethyl ester | HCID 12195 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 58266689 | HCID 58266689 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58266356 | HCID 58266356 | 14% |
Reaction Steps
To a solution of cis 4-(4-bromo-2-fluorobenzyl)-2,6-dimethylmorpholine (0.76 g, 2.5 mmol) in 1,4-dioxane (7.5 mL) under nitrogen was added ethyl urethane (1.2 mL, 10.0 mmol) followed by portionwise addition of sodium hydride (60% dispersion in mineral oil, 0.40 g, 10.0 mmol). The reaction mixture was heated at 100° C. for 24 h then partitioned between DCM and water and the phases were separated. The aqueous phase was further extracted with DCM and the combined organic layers were dried over sodium sulfate, filtered and evaporated. The residue was purified by flash chromatography (silica, 80 g column, ISCO, 0-100% ethyl acetate in pentane) to afford the title compound (0.114 g, 14%). 1H NMR (CD3OD and CDCl3, 300 MHz): 7.22 (d, J=8.0 Hz, 1H), 7.05 (dd, J=8.1, 1.9 Hz, 1H), 6.97 (d, J=1.9 Hz, 1H), 4.01 (q, J=7.0 Hz, 2H), 3.75-3.62 (m, 2H), 3.47 (s, 2H), 2.75-2.66 (m, 2H), 1.86-1.76 (m, 2H), 1.41 (t, J=7.0 Hz, 3H), 1.14 (d, J=6.3 Hz, 6H). LCMS (Method G): RT=3.24 min, M+H÷=328.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09216980B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-3542087e55c940f28876059425a13cc5 |
|---|
| Source note | uspto-grants-2015_12 |
|---|