HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4,5-Trimethoxybenzaldehyde → 1-(3,4,5-Trimethoxyphenyl)-2-propyn-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4,5-Trimethoxybenzaldehyde | HCID 6858 | — |
| Reactant | HCID 178463197 | HCID 178463197 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3,4,5-Trimethoxyphenyl)-2-propyn-1-ol | HCID 16110327 | 73.3% |
Reaction Steps
A solution of 3,4,5-trimethoxybenzaldehyde (1.0 g, 5.0 mmol) in THF (50 mL) was stirred at 0° C. Sodium acetylide (18% w.t. slurry in xylene, 1.63 g, 6.1 mmol) was added via syringe. The reaction mixture was stirred overnight at room temperature and quenched by water. It was then extracted with EtOAc (30 mL×3). The combined organic layers were washed with brine, dried over anhydrous MgSO4, filtered, and concentrated to give a crude product, which was purified by flash column chromatography eluting with EtOAc/n-hexane (1:2) to afford 1-(3,4,5-trimethoxyphenyl)prop-2-yn-1-ol as a white solid (815 mg, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07456289B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-706fa45e5dde4051bca2c44091994724 |
| Source note | uspto-grants-2008_11 |