HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 117774505, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 53632406 | HCID 53632406 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Product | HCID 117774505 | HCID 117774505 | — |
Reaction Steps
ZnBr2 (3.0 g, 13.4 mmol) was added to a solution of acetic anhydride (30 mL) and 4-methyl-tricyclo[6.2.1.0(2,7)]undec-4-ene (10.0 g, 62 mmol) and then heated under reflux. After 2 hours at reflux the mixture was cooled then poured into dilute NH4OH (6%) and extracted with diethyl ether. The organic phase was washed with saturated NaHCO3, then brine, dried over Na2SO4, filtered and the solvents removed in vacuo. The crude ketone (9.3 g orange oil) was further purified by bulb to bulb distillation 0.1 mbar at 120° C. gave the desired ketone, 5.4 g as a mixture of isomers (7:6:16:21:16).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273268B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-57e38804233741e298fa6fb7b9e71ecd |
| Source note | uspto-grants-2016_03 |