HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2-tert-Butyl-5-(propan-2-ylidene)cyclopenta-1,3-diene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Tert-butylcyclopentadiene | HCID 633714 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-tert-Butyl-5-(propan-2-ylidene)cyclopenta-1,3-diene | HCID 14688283 | 90.8% |
Reaction Steps
To a mixed solution of 1.40 g (11 mmol) of tert-butylcyclopentadiene, 8.4 ml (114 mmol) of acetone and 20 ml of methanol, 9.5 ml (114 mmol) of pyrrolidine was added with ice cooling, followed by stirring at room temperature for one night. To the reaction solution, 50 ml of water, 100 ml of ether and 3 ml of acetic acid were added with ice cooling. The separated organic phase was washed with water and dried over anhydrous sodium sulfate. After the solvent was distilled off, the residue was subjected to column chromatography (silica gel, developing solvent: hexane) to obtain 1.62 g of a yellow liquid (yield: 88%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07449533B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-cb5d1c826d7e47cb80af0dfe7127fa08 |
| Source note | uspto-grants-2008_11 |