HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetaldehyde → t-Butyl 4-phenyl-2-butenoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetaldehyde | HCID 998 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl diethylphosphonoacetate | HCID 2773685 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | t-Butyl 4-phenyl-2-butenoate | HCID 53401901 | 69.3% |
Reaction Steps
To a solution of 12.15 mL (45.78 mmol) of t-butyldiethylphosphonoacetate in 100 mL of THF under argon at 25° C. is added 1.83 g (45.78 mmol) of 60% NaH in oil dispersion. The reaction mixture is stirred at 25° C. for 45 minutes at which time 5.41 mL (41.62 mmol) of phenylacetaldehyde is added. After 30 minutes at 25° C. the reaction is partitioned between 1 N HCl and ethyl ether. The organic layer is dried over anhydrous MgSO4 and concentrated in vacuo. Purification by flash silica gel chromatography affords 6.3 g (69%) of t-butyl 4-phenylbut-2-enoate as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057369 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-722fdd3a62bc411a9afdc5a2f5fc55d0 |
| Source note | uspto-grants-2000_05 |