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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620552Generated: October 24, 2026

Carbon tetrabromide → 1-Undecyne, 11-bromo-

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Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant10-Undecyn-1-olHCID 76015—
SolventDichloromethaneHCID 6344—
Product1-Undecyne, 11-bromo-HCID 11711152.4%

Reaction Conditions

Temperature0 °C

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-292843c0651a46d6aea910a8132274c6
Source noteuspto-grants-1989_04