HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 67547382, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 13124210 | HCID 13124210 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67547382 | HCID 67547382 | — |
Reaction Steps
To a solution of 7-methoxy-2,2-dimethyl-3,4-dihydro-2H-naphthalen-1-ol (1.40 g, 6.52 mmol) and DMAP (0.16 g, 1.30 mmol) in dichloromethane (30 mL) is added triethylamine (1.99 g, 19.55 mmol) and acetic anhydride (1.68 g, 16.29 mmol). After 45 min, the mixture is diluted with ethyl acetate and washed successively with 1M aqueous sodium bisulfate, saturated aqueous sodium bicarbonate, and brine. The organic phase is dried over magnesium sulfate, filtered, and concentrated to give acetic acid 7-methoxy-2,2-dimethyl-1,2,3,4-tetrahydro-naphthalen-1-yl ester, which is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436035B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-fab86800d0224cd1805c35c4bf544b46 |
| Source note | uspto-grants-2013_05 |