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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273343Generated: October 25, 2026

3,4,5-Trimethoxybenzaldehyde → 1-(3,4,5-Trimethoxyphenyl)-2-propyn-1-ol

https://huagongshe.com/reaction/273343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantHCID 178463197HCID 178463197—
SolventTetrahydrofuranHCID 8028—
Product1-(3,4,5-Trimethoxyphenyl)-2-propyn-1-olHCID 1611032773.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456289B2
Source datasetuspto-grants-2008_11
ORD IDord-706fa45e5dde4051bca2c44091994724
Source noteuspto-grants-2008_11