HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651834Generated: October 31, 2026
3,4,5-Trimethoxybenzaldehyde → HCID 23050479, compound
https://huagongshe.com/reaction/1651834
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4,5-Trimethoxybenzaldehyde | HCID 6858 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 23050500 | HCID 23050500 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23050479 | HCID 23050479 | — |
Reaction Steps
A solution of 10 g (58 mmol) of 2-(2-methoxyethoxy)ethyl propiolate in 80 ml of tetrahydrofuran was treated at -78° under argon with 36 ml of n-butyllithium (1.6M in hexane). The mixture was stirred at -78° for 10 minutes and then a solution of 11.4 g (58 mmol) of 3,4,5-trimethoxy-benzaldehyde in 60 ml of tetrahydrofuran was added within 30 minutes. The reaction mixture was stirred at -78° for a further 30 minutes, then brought to room temperature and treated with 150 ml of saturated ammonium chloride solution. The aqueous phase was extracted twice with ether. The combined organic phases were washed in succession with saturated sodium chloride solution and with water, dried over sodium sulphate and concentrated. The residue was purified by flash chromatography on 1000 g of silica gel (elution agent methylene chloride/ether 4:1). There was obtained 2-(2-methoxyethoxy)ethyl 4-hydroxy-4-(3,4,5-trimethoxyphenyl)-2-butynoate as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04929741 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-004523e4b1fe4094ba90585e8fe9759d |
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| Source note | uspto-grants-1990_05 |
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