HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylcyclohexanone → Cyclohexane, 1-(1,1-dimethylethyl)-4-methylene-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylcyclohexanone | HCID 7392 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Cyclohexane, 1-(1,1-dimethylethyl)-4-methylene- | HCID 139425 | 70% |
Reaction Steps
BDAM (3.00 grams) was suspended in 40 milliliters of methylene chloride and 2 molar equivalents of THF were added at 0° C. After a homogeneous solution was formed, 1 molar equivalent of TEAL in 10 milliliters of hexane was added followed by 2.20 grams of 4-tert-butylcyclohexanone. After overnight stirring, reaction mixture was hydrolyzed and worked up as described in Example 1. A total of 1.50 grams of 4-tert-butyl-1-methylenecyclohexane was isolated (70% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04849574 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-e97d4a423c634dc3b47fab2cc27e75c0 |
| Source note | uspto-grants-1989_07 |