HuagongsheHuagongshe Chemistry Print Report · For research reference only
Camphor → 2,2-Diethoxy-1,7,7-trimethylbicyclo[2.2.1]heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Camphor | HCID 2537 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,2-Diethoxy-1,7,7-trimethylbicyclo[2.2.1]heptane | HCID 68158850 | — |
Reaction Steps
To a flask with reflux condenser, (25 g) camphor and 50 ml absolute ethanol was taken. (36.45 g) (1.5 eq.) triethyl orthoformate and crystals of p-toluenesulfonic acid was added into the reaction mixture. The reaction mixture was heated to reflux overnight. The reaction mixture was cooled and concentrated on rotavapour and was washed with 10% potassium hydroxide solution. Extract it with dichloromethane and concentrated the organic layer on rotavapour, yellow colored liquid product was obtained. 38. g (Quantitative)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754207B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-dbc7cbb7aa4c47da93c472fe11353096 |
| Source note | uspto-grants-2014_06 |