HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzaldehyde → Cyclohexyl-(4-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | HCID 178419651 | HCID 178419651 | — |
| Product | Cyclohexyl-(4-methoxyphenyl)methanol | HCID 9920862 | — |
Reaction Steps
Referring now to FIG. 2, this alternative synthesis starts from 4-methoxy-benzaldehyde (VI) which is subjected to treatment with cyclohexyl magnesium bromide to yield cyclohexyl-(4-methoxy-phenyl)-methanol (V). This in turn is then oxidised so as to yield cyclohexyl-(4-methoxy-phenyl)-methanone (III).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06756502B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-aacd95c11a9f4f8eb70c139deb24342e |
| Source note | uspto-grants-2004_06 |