HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 2-(1-Fluoro 2-propynyl)-4-thiazolemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | alpha-ethynyl 4-[[(tetrahydro 2H-pyran-2-yl) oxy] methyl] 2-thiazole methanol | HCID 53736243 | — |
| Reactant | Diethylaminosulfide trifluoride | HCID 86605672 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1-Fluoro 2-propynyl)-4-thiazolemethanol | HCID 20086714 | — |
Reaction Conditions
| Temperature | -55 °C |
|---|
Reaction Steps
0.53 ml of diethylaminosulfide trifluoride (DAST) were added at about -60° C. to a solution of 1 g of the product of Stage C and 5 ml of methylene chloride and the reaction mixture was stirred for 2 hours at -55° C. and poured into a solution of sodium bicarbonate. Extraction was carried out with methylene chloride and the extracts were dried over magnesium sulfate, filtered and evaporated to dryness. The residue was taken up in 5 ml of methanol and 20 mg of toluene-sulfonic acid were added. The reaction mixture was stirred for one hour at 20° C., followed by evaporation to dryness. The residue was chromatographed on silica eluting with a hexane-ethyl acetate mixture (7-3) to obtain 0.16 g of the desired product with a Rf=0.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05395845 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-28169f9ea77941eea284bc7229c3d666 |
| Source note | uspto-grants-1995_03 |