HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 10447045, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 10131175 | HCID 10131175 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 10447045 | HCID 10447045 | 81% |
Reaction Steps
To a solution of 5-hydroxy-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-3-carboxylic acid (25.03 g, 100 mmol) in pyridine (200 mL) is added acetic anhydride (100 mL) and the mixture is stirred at room temperature for 24 hrs. Water and ice are added and the mixture is stirred at about 30° C. for 30 min. The mixture is cooled in ice and 6N hydrochloric acid (450 mL) is added. The resulting solid is collected, washed with water, taken up in ethyl acetate. The organic layer is washed with 2N hydrochloric acid and water, dried (sodium sulfate) and evaporated to dryness. Recrystallization from ethyl acetate gave 23.6 g (81%) of 5-acetoxy-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-3-carboxylic acid (mp=187° C.-188° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05698696 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-11d2f3012a3f4018b58f925b6d1e2f86 |
| Source note | uspto-grants-1997_12 |