HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Pentanol → Diisopentyl carbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Pentanol | HCID 6276 | — |
| Reactant | Isoamyl carbamate | HCID 10984 | — |
| Reactant | Pentyl carbamate | HCID 69490 | — |
| Reactant | HCID 66621985 | HCID 66621985 | — |
| Solvent | Isoamyl Alcohol | HCID 31260 | — |
| Product | Diisopentyl carbonate | HCID 74913 | 89% |
Reaction Steps
The procedure described in Example 4 is followed, but the n-pentanol and n-pentyl carbamate are replaced respectively by isoamyl alcohol and isoamyl carbamate, and diazabicyclo-[4,3,0]-nonene is used as the catalyst. After completion of the reaction, analysis by gas chromatography shows that 66.9% of isoamyl carbamate have been converted and 120.3 parts of diisoamyl carbonate (89% of theory, based on converted isoamyl carbamate), of boiling point 106°-108° C./18 mbar, have been formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04436668 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-4bf290f41c1a4134b7f574cacdd973dc |
| Source note | uspto-grants-1984_03 |