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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888440Generated: November 2, 2026

Carbamic acid, ethyl-, ethyl ester → HCID 58266356, compound

https://huagongshe.com/reaction/1888440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbamic acid, ethyl-, ethyl esterHCID 12195—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58266689HCID 58266689—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58266356HCID 5826635614%

Reaction Conditions

Temperature100 °C

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, 1 H), 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, 2 H), 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-aa327d618dfb4c4291412c26f416f496
Source noteuspto-grants-2013_08