HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 4,4-Diethoxy-1-phenyl-but-2-yn-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 3,3-Diethoxypropyne | HCID 66285 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4-Diethoxy-1-phenyl-but-2-yn-1-ol | HCID 10889848 | — |
Reaction Steps
A mixture of 3,3-Diethoxy-propyne (4.55 g, 35.5 mmol) in THF (90 mL) was cooled to −78 C under N2. A solution of n-BuLi (2.0M in cyclohexane, 24 mL, 46 mmol) was added. After 30 min., Benzaldehyde (4.90 g, 46 mmol) was added. After 15 h, the reaction was quenched by dilution with 1N HCl, warmed to room temperature and extracted into EtOAc. The organic layer was washed with brine, dried over sodium sulfate, filtered and evaporated to give product, 9.46 g (88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08404859B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-024ff8da6f5a4700b807401aec25200e |
| Source note | uspto-grants-2013_03 |