Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | 2-Ethylhexanol | HCID 7720 | — |
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Dibutyltin oxide | HCID 61221 | — |
| Product | HCID 18954420 | HCID 18954420 | — |
Reaction Steps
225 g (3.0 mols) of 2-methoxyethylamine, 180 g (3.0 mols) of urea, 1,950 g (15 mols) of 2-ethylhexanol and 3 g of dibutyltin oxide are introduced into a 4 liter round-bottom flask equipped with reflux condenser, and the mixture is heated while stirring. A vigorous evolution of ammonia sets in at temperatures above 110° C. Ammonia gas is removed through the reflux condenser and absorbed in water. Over the course of 3 hours, the temperature is increased to 180° C. (reflux), the elimination of ammonia virtually ceasing. After a further 2 hours under reflux, the mixture is freed of remaining ammonia by flushing with nitrogen and subsequently subjected to fractional distillation. After a first cut comprising mainly ethylhexanol, the desired urethane distills over at 98°-100° C./0.1 mbar as a colorless liquid (yield: 617 g=89% of theory). 27 g of a brown liquid remain as the distillation residue and solidify to give a pasty product on cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05371271 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-159029874f4547bdab799f0af2fe3275 |
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| Source note | uspto-grants-1994_12 |
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