HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydroxybutanedioic Acid → HCID 102020809, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | D-Tartaric acid | HCID 439655 | — |
| Reactant | HCID 129631015 | HCID 129631015 | — |
| Product | HCID 102020809 | HCID 102020809 | — |
Reaction Steps
Diacetyl-L-tartaric anhydride is prepared from D-tartaric acid in the manner described in "DIACETYL-d-TARTARIC ANHYDRIDE (Tartaric anhydride, diacetate of d-)", Organic Synthesis, Collective Volume 4, 242-243 (1963). Briefly, a tartaric acid isomer or mixture of isomers is treated with acetic anhydride with a catalytic amount of sulfuric acid. The solution is heated gently for about 10 minutes and poured into an ice bath. The crystalline material formed is collected on a filter and is washed with toluene and ether and dried over phosphorus pentoxide and paraffin shavings. The crystalline bisacetyltartaric anhydride is used as is described in the following paragraph.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05604220 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-7f25c643d0354ca38ccb81944882f0cf |
| Source note | uspto-grants-1997_02 |