HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (4-Chlorophenyl)(4-cyanophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | HCID 178467826 | HCID 178467826 | — |
| Solvent | Carbon dioxide methanol | HCID 21973728 | — |
| Product | (4-Chlorophenyl)(4-cyanophenyl)methanol | HCID 67001080 | 96% |
Reaction Steps
To a solution of 4-cyanobenzaldehyde (3.93 g) in tetrahydrofaran was added dropwise 1.0M 4-chlorophenylmagnesium bromide-diethylether (30 mL) under nitrogen gas atmosphere and cooling in dry ice/methanol bath and the mixture was stirred at the same temperature for 10 minutes. To the reaction mixture was added 10% HCl solution and the aqueous layer was extracted with ethyl acetate (×2). The organic layer was washed with a saturated brine, dried over magnesium sulfate and concentrated in vacuo. To the resultant crude product was added diisopropyl ether and the resultant solid materials were collected by filtration to give (4-chlorophenyl)(4-cyanophenyl)methanol (6.98 g, yield: 96%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08034949B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-79a58ad7274a4720b057ffb930410173 |
| Source note | uspto-grants-2011_10 |