Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620553Generated: October 25, 2026

Salicylaldehyde → 2-(10-Undecynyloxy)benzaldehyde

https://huagongshe.com/reaction/620553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Undecyne, 11-bromo-HCID 117111—
SolventDimethylformamideHCID 6228—
Product2-(10-Undecynyloxy)benzaldehydeHCID 15617498—

Reaction Steps

To an ice-cold solution of 11-hydroxyundecyne (10 g, 59.4 mmoles) in 400 ml of methylene chloride under argon was added in one portion carbon tetrabromide (40.5 g, 0.1224 mole). The reaction mixture was stirred at 0° C. for 5 minutes and triphenylphosphine (29.43 g, 0.1122 mole) was added. The reaction was kept at 0° C. for an additional 15 minutes and stirred at room temperature for 3 hours. The methylene chloride was removed in vacuo. The residue was treated with hexane and the combined organic extract was concentrated in vacuo. The crude product was purified by flash chromatography on silica, eluting with straight hexane, to give 7.2 g (52%) of 11-bromoundecyne as a colorless oil. Following the procedures of Examples 20 and 39(a), a mixture of salicylaldehyde, 11-bromoundecyne and potassium carbonate in dimethylformamide is reacted to furnish 2-(10-undecynyloxy)benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820719
Source datasetuspto-grants-1989_04
ORD IDord-42b36ef54d034d21a8378d05ae0d03bc
Source noteuspto-grants-1989_04