HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21996494, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 7-Amino-1,2,3,4-tetrahydronaphthalen-1-one | HCID 327177 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 21996494 | HCID 21996494 | 91% |
Reaction Steps
To a solution of 7-amino-1-tetralone (1.70 g, 10.5 mmol) in formic acid (3 ml) was added a mixture of formic acid (8 ml) and acetic anhydride (3 ml), followed by stirring for 10 minutes at room temperature. The reaction mixture was concentrated under reduced pressure. The concentrate was neutralized with a saturated aqueous solution of sodium hydrogencarbonate, which was subjected to extraction with ethyl acetate. The extract solution was washed with brine and dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The residue was recrystallized from ethyl acetate/isopropyl ether to give 1.80 g (yield 91%) of the above-titled compound, m.p.137-138° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235789B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-811ae20377ff4461bdfd6b8fbb6260a8 |
| Source note | uspto-grants-2001_05 |