HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinone → HCID 12657569, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinone | HCID 4650 | — |
| Reactant | 1,3-Cycloheptadiene | HCID 19969 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12657569 | HCID 12657569 | — |
Reaction Steps
To a solution of 17.2 g of 1,4-benzoquinone in 240 mL DCM were added 7.6 mL of BF3-diethyletherate followed by 17.2 mL of 1,3-cycloheptadiene at −20° C. The cooling bath was removed after 20 min and the mixture furthermore stirred for 30 min at rt. The reaction mixture was then poured into ice cold KOH (30% aq.) solution and it was vigorously stirred for 10 min. After filtration over celite the organic phase was dried over K2CO3 and concentrated in vacuo to obtain 21.7 g of the desired compound as mixture of stereoisomers as brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314253B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-6a908e6b462d4d7aa16ec6c1d149f4ff |
| Source note | uspto-grants-2012_11 |