HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dihydroxyacetone → 1,3-Dibutyrin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dihydroxyacetone | HCID 670 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1,3-Dibutyrin | HCID 122920 | — |
Reaction Steps
By following the procedure of Example 1(a) and 1(b) using 13.05 g. of 1,3-dihydroxyacetone, 23.7 g. of pyridine and 31.1 g. of butyryl chloride, 17.9 g. of 1,3-dibutanoyloxy-2-propanol is obtained. The reaction of 12.2 g. of this material and 9.4 g. of valproyl chloride and 4.98 g. of pyridine as described in Example 1(c) yields an oil which is purified by chromatography as described in Example 3. The pure 1,3-dibutanoyl-2-valproyl-glyceride is eluted from the column with petroleum ether/ether (95:5); it is obtained in a yield of 9.1 g.; Rf 0.61 (petroleum ether/ether 3:1); mass spectrum m/e 316 (M+ -42).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04654370 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-0d533ae828c945839b89498cd6af0d14 |
| Source note | uspto-grants-1987_03 |