HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 15617823, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 6,6,6-Trimethoxyhex-1-yne | HCID 13096567 | — |
| Reactant | 1-(Benzyloxy)-2-naphthaldehyde | HCID 15617822 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15617823 | HCID 15617823 | 98.9% |
Reaction Steps
A solution of 1,1,1-trimethoxy-5-hexyne (3.90 g, 0.023 mo)e) in dry tetrahydrofuran (50 mL) was stirred at -78° and treated with n-butyllithium (1.6M in hexane; 15 mL, 0.024 mole). The solution was stirred for 30 minutes, then treated with a solution of 1-benzyloxy-2-naphthaldehyde (4.25 g. 0.016 mole) in dry tetrahydrofuran (12 mL). The reaction mixture was allowed to warm to room temperature, stirred for 4 hours, and poured into water. The crude product was isolated by extraction with ether and chromatographed with 3:1 ether/hexane. This afforded the title compound (6.15 g. 97%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985442 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-336a580fd2eb4cf58cbd08d514395a31 |
| Source note | uspto-grants-1991_01 |