HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → (2R)-5-(Acetyloxy)tetrahydro-2-thiophenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 1-O-Acetyl-5-O-t-butyldiphenylsilyl-4-thio-2,3-dideoxyribofuranose | HCID 15126098 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2R)-5-(Acetyloxy)tetrahydro-2-thiophenemethanol | HCID 54182721 | 71.5% |
Reaction Steps
To a mixture of 0.54 g of 1-O-acetyl-5-O-(tert-butyldiphenylsilyl)-2,3-dideoxy-4-thioribofuranose (prepared by the procedure of J. A. Secrist et al., J. Meal. Chem.,1992, 35, 533) in 8 ml of tetrahydrofuran and 0.6 g of acetic acid is added 4 mmol of 1M n-tetrabutylammonium fluoride solution. The reaction is stirred for 5 hours and then another portion of 0.10 g of acetic acid and I mmol of n-tetrabutylammonium fluoride is added and the reaction is stirred for 1 hour. Cold potassium dihydrogen phosphate and ethyl acetate are added to the reaction mixture, followed by an aqueous workup. Purification by chromatography gives 0.164 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05623081 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-a99e727574c344ae8230b4534d34b25e |
| Source note | uspto-grants-1997_04 |