HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 16100288, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Adamantane | HCID 9238 | — |
| Reactant | Delta-Valerolactone | HCID 10953 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 16100288 | HCID 16100288 | — |
Reaction Steps
A solution of 3.6 mL (25 mmol) of Et3N in 6.7 mL of 1,2-dichloroethane was added drop by drop under ice cooling to a suspension of 2.47 g (18.3 mmol) AlCl3 in 13.3 mL of dichloroethane. At room temperature a solution of 2.77 g (18.3 mmol) adamantane and 1.55 mL (16.7 mmol) delta-valerolactone in 10 mL of 1,2-dichloroethane was added to the mixture. After one hour of stirring at room temperature the mixture was quenched with ice water and stirred for another 30 minutes. The suspension was filtered by Celite. After addition of dichloromethane, separation of the organic layer, washing it with water, drying it with Na2SO4 and the solvent was evaporated. The product can be taken for further reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389555B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-da23858761db448294a3d27a0dbd95c1 |
| Source note | uspto-grants-2013_03 |