HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19478Generated: October 29, 2026
Formaldehyde → N-ethyl-N-(hydroxymethyl)urethane
https://huagongshe.com/reaction/19478
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Carbamic acid, ethyl-, ethyl ester | HCID 12195 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-ethyl-N-(hydroxymethyl)urethane | HCID 21453680 | 99.3% |
Reaction Steps
Under general experimental conditions reported by Kelper, JOC, 52, 453-55 (1987), a slurry of Ba(OH)2 (46.0 mg, 266 μmol) in water (480 μL) was added to a mixture of N-ethylurethane (2.04 mL, 17.1 mmol) and a 37% aqueous solution of formalin (1.28 mL, 17.1 mmol) in one portion with stirring. The mixture became cool and gradually formed a cloudy solution. The mixture was stirred at room temperature and the disappearance of N-ethylurethane monitored by TLC analysis. After 2 h, the reaction was quenched by adding solid CO2, stirred for 30 minutes and filtered to remove the precipitated barium carbonate. The solvent was removed under vacuum to provide an oily residue. The trace amounts of water were removed by azeotropic distillation with benzene (3×100 mL) to provide 56 as a clear oil (2.50 g, quant.): 1H NMR (400 MHz, CDCl3) δ 4.88 (d, J=7.6 Hz, 1H), 4.79 (d, J=7.6 Hz, 2H), 4.18 (q, J=7.6 Hz, 2H), 3.40 (q, J=6.4 Hz, 2H), 1.30 (t, J=7.6 Hz, 3H), 1.19 (t, J=7.6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745415B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-6d03d557d822487c9712e8910830927c |
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| Source note | uspto-grants-2010_06 |
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