HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 19772508, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1,2,3,4-Tetrahydro-1,4-methanonaphthalene | HCID 138272 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | HCID 19772508 | HCID 19772508 | — |
Reaction Steps
30 cm3 of acetyl chloride are added to a solution of 30 g of benzonorbornene in 400 cm3 of carbon disulphide and then 10.5 g of anhydrous aluminum chloride are added gradually in small quantities over approximately 2 hours. At this stage, the complete conversion of the starting product is checked by thin-layer chromatography. The reaction mixture is then poured into two litres of ice water and then neutralized with sodium bicarbonate. After three extractions with ether, the ether phase is dried over sodium sulphate and then concentrated. 38 g of an orange oil which corresponds to the expected product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05198567 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-6678837d21604da7beff53638898a47d |
| Source note | uspto-grants-1993_03 |