HuagongsheHuagongshe Chemistry Print Report · For research reference only
beta(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol → alpha(S)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | beta(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol | HCID 53702433 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | alpha(S)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-acetaldehyde | HCID 22856132 | 77.9% |
Reaction Steps
15.0 g of pyridinium chlorochromate and 10.0 g of crushed 3A molecular sieves were added to a solution of 5.50 g (0.019 mol) of β(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol in 200 ml of dichloromethane. The mixture was stirred at room temperature for 20 hours, then diluted with 200 ml of diethyl ether and filtered. The filtrate was evaporated to give 4.30 g of α(S)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-acetaldehyde which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05516913 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-7abb0e9c6a7a4d72981bf6e994fab3dc |
| Source note | uspto-grants-1996_05 |