HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 54042579, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 57195921 | HCID 57195921 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54042579 | HCID 54042579 | 85.9% |
Reaction Steps
20.0 g (46.8 mmol) of t-butyl (4S,5S)-4-(cyclohexylmethyl)-5-[(2S,3RS)-3,4-dihydroxy-2-isopropylbutyl]-2,2-dimethyl-3-oxazolidinecarboxylate are dissolved in 250 ml of benzene, cooled to 5° and treated portionwise within 10 minutes with 20.8 g (47 mmol) of lead tetraacetate. After stirring at 5° for 4 hours 500 ml of ether are added and the reaction mixture is stirred for a further 15 minutes. Thereafter, the reaction mixture is filtered and the filtrate is evaporated under reduced pressure. Chromatography of the residue on 300 g of silica gel with methylene chloride as the eluting agent yields 15.9 g of t-butyl (4S,5S)-4-(cyclohexylmethyl)-5-[(S)-2-formyl-3-methylbutyl]-2,2-dimethyl-3-oxazolidinecarboxylate as an oil, MS: 380 (M-CH3)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05140011 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-63d2ab3961454edbbce8fb26fe7f799b |
| Source note | uspto-grants-1992_08 |