HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 12813111, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 12813134 | HCID 12813134 | — |
| Product | HCID 12813111 | HCID 12813111 | — |
Reaction Steps
A solution of 51 g of 1,6-anhydro-3,4-di-O-benzyl-2-O-tetrahydropyranyl-β-D-glucopyranose in 400 ml of acetone is warmed with 20 ml 1 N hydrochloric acid to 50° for 20 minutes. After cooling, this solution is neutralised with 1 N sodium hydroxide solution and evaporated to dryness. The residue is taken up in ether, this solution is washed thoroughly with water and dried over magnesium sulphate and the solvent is evaporated. The product is benzoylated as described in Example 3 and the 1,6-anhydro-2-O-benzoyl-3,4-di-O-benzyl-β-D-glucopyranose which is thus obtained is purified by recrystallisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04177344 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-cb56844ec5d7429f85926690087a7e57 |
| Source note | uspto-grants-1979_12 |