HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22916681, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 15428311 | HCID 15428311 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22916681 | HCID 22916681 | 95% |
Reaction Steps
0.15 g of the 3-hydroxymethylimidazo[5,1-b]thiazole prepared in Preparation 55 was dissolved in 4 ml of dichloromethane, and the solution was stirred. To this was added 0.1 ml of acetic anhydride, and the mixture was stirred at room temperature for 3 hours. To the reaction solution was added 5 ml of a saturated aqueous solution of sodium hydrogencarbonate, and the organic layer was separated. The aqueous layer was extracted with dichloromethane (5 ml×2). The combined organic layers were dried over anhydrous magnesium sulfate, and concentrated to dryness under reduced pressure to give 0.181 g (yield 95%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663162 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-0f70cdc3e5954167b9031c7169948e14 |
| Source note | uspto-grants-1997_09 |