HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-(4-Bromophenyl)cyclohexane-1-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Bromo-4-[4-(methoxymethylidene)cyclohexyl]benzene | HCID 19097914 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Bromophenyl)cyclohexane-1-carbaldehyde | HCID 19097901 | 95.1% |
Reaction Steps
A mixture of 10.4 g of 1-bromo-4-[4-(methoxymethyli-dene)cyclohexyl]benzene and 100 ml of tetrahydrofuran/2N hydrochloric acid (vol. 4:1) was heated to reflux for 30 minutes in a round flask. Subsequently, the reaction mixture was poured into 100 ml of water and extracted three times with 100 ml of diethyl ether each time. The organic phases were washed with 100 ml of water, dried over magnesium sulphate and concentrated. There were obtained 9.4 g of 4-(4-bromophenyl)cyclohexanecarboxaldehyde as white crystals; trans/cis ratio about 5:3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05288428 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-1ccd38fd5d124569bac9e683f3bf82a6 |
| Source note | uspto-grants-1994_02 |