HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651790Generated: November 2, 2026
4-Hydroxybenzaldehyde → HCID 23050521, compound
https://huagongshe.com/reaction/1651790
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Propyne, 3-(1-ethoxyethoxy)- | HCID 86774 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23050521 | HCID 23050521 | — |
Reaction Steps
A solution of 16 g (124.8 mmol) of 1-(1-ethoxyethoxy)-2-propyne in 270 ml of tetrahydrofuran was treated at -78° under argon with 78 ml of n-butyllithium (1.6 M in hexane). The mixture was stirred at -40° for 30 minutes and then a solution 7.62 g (62.4 mmol) of 4-hydroxybenzaldehyde in 53 ml of tetrahydrofuran was added within 10 minutes. The reaction mixture was warmed to 0°, stirred at 0° for a further 1 hour and then treated with 100 ml of saturated ammonium chloride solution. The aqueous phase was extracted twice with ethyl acetate. The combined organic phases were washed in succession with saturated sodium chloride solution and with water, dried over magnesium sulphate and concentrated. The residue was purified by flash chromatography on 600 g of silica gel (elution agent ether/hexane 1:1). There was obtained 4-(1-ethoxyethoxy)-(4-hydroxyphenyl)-2-butyn-1-ol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04929741 |
|---|
| Source dataset | uspto-grants-1990_05 |
|---|
| ORD ID | ord-5fb2dee539de4ff1ab38e274bd3ffb71 |
|---|
| Source note | uspto-grants-1990_05 |
|---|