HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → HCID 53990429, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | HCID 68122688 | HCID 68122688 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53990429 | HCID 53990429 | — |
Reaction Steps
A mixture of 10.4 g (0.027 mole) of 2-(5-tetradecyloxy)thenoylacetic acid, 4.4 g (0.027 mole) of N,N'-carbonyldiimidazole, and anhydrous tetrahydrofuran is stirred until the evolution of carbon dioxide gas stops. The mixture is cooled on an ice bath, in 3.0 g (0.027 mole) of benzyl alcohol is added. The reaction is allowed to warm to room temperature and evaporated to dryness. The residue is extracted with ether-H2O. The ether layer is washed with 10% aqueous HCl, then water, then saturated sodium chloride, dried with sodium sulfate and evaporated to dryness to give 5-tetradecyloxythen-2-oylacetic acid benzyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04032647 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-9b4f6c6476ea46b1be1fa39eb534d584 |
| Source note | uspto-grants-1977_06 |