HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxy-4-methylbenzaldehyde → HCID 68714672, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxy-4-methylbenzaldehyde | HCID 585182 | — |
| Reactant | HCID 22161009 | HCID 22161009 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 68714672 | HCID 68714672 | 88.2% |
Reaction Steps
Under an atmosphere of Argon, to a solution of n-hexylphosphonium bromide (1.07 g) in tetrahydrofuran (10 mL) was added potassium t-butoxide (336 mg) at room temperature and the solution was stirred for 30 minutes. After cooling in ice bath, 3-hydroxy-4-methylbenzaldehyde (136 mg) was added to the reaction solution, which was stirred at room temperature for 1.5 hours. The reaction solution was diluted with t-butyl methyl ether. The solution was washed with dilute hydrochloric acid, water and brine, dried over anhydrous sodium sulfate and concentrated. The obtained residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:4) to give the title compound (180 mg) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858650B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-23ca5c06538a48a2ba8344d32965c41a |
| Source note | uspto-grants-2010_12 |