HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → (5S)-5-{[(tert-butyldimethylsilyl)oxy]methyl}oxolan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (S)-(+)-gamma-Hydroxymethyl-gamma-butyrolactone | HCID 2733813 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (5S)-5-{[(tert-butyldimethylsilyl)oxy]methyl}oxolan-2-one | HCID 10014094 | 90% |
Reaction Steps
A solution of 13.2 g (113 mmol) of (5S)-dihydro-5-(hydroxymethyl)furan-2(3H)-one in 200 ml of dimethyiformamide was treated sequentially with 9.28 g (136 mmol) of imidazole and 18.84 g (125 mmol) of chloro-t-butyldimethylsilane, the latter in several portions. The resulting solution was stirred at ambient temperature for 6 h, poured into 10% aqueous citric acid, and extracted with ethyl acetate. The organic layer was washed sequentially with two portions of water, one portion of aqueous NaHCO3 and one portion of saturated brine. The organic layer was dried over MgSO4, and concentrated in vacuo to provide 22.04 g (90%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05455351 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-5e693f7ec1d94189802182bf08225e87 |
| Source note | uspto-grants-1995_10 |