Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Trimethylolhexane | HCID 13760613 | — |
| Product | 3-Amyl-3-hydroxymethyloxetane | HCID 18673215 | 24.4% |
Reaction Steps
84.5 mmoles of trimethylolhexane and 70.9 mmoles of carbamide were together with 1.2 mole % of potassium hydroxide (based on total amount of reactants and catalysts) charged in a reaction vessel. The synthesis was performed in accordance with Example 1. The temperature uring the pyrolysis gradually raised to 215° C. 20.6 mmoles of 3-hydroxymethyl-3-pentyloxetane (trimethylolhexane oxetane) was yielded from the distillate and characterised by NMR. The remainder contained the spiro-orthocarbonate (3% on the carbamide) yielded as by-product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515152B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-01f51a6f0f1b4129801b9e83bb1b7562 |
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| Source note | uspto-grants-2003_02 |
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