HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → HCID 21535782, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | 3-Methylbut-1-yne | HCID 69019 | — |
| Reactant | tert-Butyl ethyl ethanedioate | HCID 14648212 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506794 | HCID 178506794 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21535782 | HCID 21535782 | — |
Reaction Steps
Ethyl t-butyl oxalate ##EQU1## can be prepared by the method of Carpino [J. Amer. Chem. Soc. 82: 2725 (1960)], and 1-lithio-3-methylbut-1-yne ##EQU2## can be prepared by reacting commercially available 3-methylbut-1-yne and n-butyllithium under anhydrous conditions in an inert atmosphere (i.e., no H2O, O2, or CO2) at a temperature of from 0° to 5° C. Anhydrous tetrahydrofuran (THF) is the preferred solvent for the reactions of step (a).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959312 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-51c1aeb0d88d483cafa9e823a224a5b1 |
| Source note | uspto-grants-1976_05 |