HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydrofuran → 1,3-O-di-(t-butyldimethylsilyl)-2-O-tetrahydrofuranylglycerol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydrofuran | HCID 70934 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | 4,8-Dioxa-3,9-disilaundecan-6-ol, 2,2,3,3,9,9,10,10-octamethyl- | HCID 10758091 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1,3-O-di-(t-butyldimethylsilyl)-2-O-tetrahydrofuranylglycerol | HCID 19361264 | 100% |
Reaction Steps
In dioxane was dissolved 3.45 g (11 mmol) of 1,3-O-di-(t-butyldimethylsilyl)glycerol followed by addition of 3.03 g (12 mmol) of pyridinium p-toluenesulfonate. To this suspension was added 16.5 ml (22 mmol) of dihydrofuran gradually under ice-cooling and the mixture was stirred for 1 hour. After return to ambient temperature, the mixture was allowed to react overnight. After completion of the reaction, the solvent was distilled off and the residue was treated with methylene chloride and saturated aqueous sodium hydrogen carbonate solution. The methylene chloride layer was washed with water, dried, and concentrated to provide 4.25 g (100%) of 1,3-O-di-(t-butyldimethylsilyl)-2-O-tetrahydrofuranylglycerol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06020317 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-452df22ba2ee4de9a642527daadbff43 |
| Source note | uspto-grants-2000_02 |