HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 15814063, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | HCID 14157593 | HCID 14157593 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | HCID 15814063 | HCID 15814063 | — |
Reaction Steps
A mixture of 25.0 g of acetyl bromide and 42.0 g of (4R,5R)-4,5-bis(acetoxymethyl)-1,3-dioxolane obtained in Example 4 was stirred under cooling with ice, and 1.0 g of anhydrous zinc chloride was added to it. After the reaction for 30 minutes, the ice water bath was dismantled and the mixture was stirred for a further one hour while stirring at room temperature. After the reaction, 50 ml of benzene was added to separate insoluble matters by filtration, and the benzene was evaporated at a low temperature (below room temperature). No peaks for the raw material were observed at all by NMR analysis of the reaction product, indicating that the decylization occurred quantitatively and the title compound was produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05532380 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-146d69ee01534e39bef6252909f41707 |
| Source note | uspto-grants-1996_07 |