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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229716Generated: October 26, 2026

1-Dodecyne → 5-(Dodec-1-YN-1-YL)-2-hydroxybenzene-1,3-dicarbaldehyde

https://huagongshe.com/reaction/229716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-DodecyneHCID 69821—
Reactant5-Bromo-2-hydroxybenzene-1,3-dicarbaldehydeHCID 5260206—
CatalystHCID 178419050HCID 178419050—
SolventAcetonitrileHCID 6342—
Product5-(Dodec-1-YN-1-YL)-2-hydroxybenzene-1,3-dicarbaldehydeHCID 5971086546%

Reaction Conditions

Temperature80 °C

Reaction Steps

2,6-Diformyl-4-bromophenol (2.50 g, 10.9 mmol), 1-dodecyne (2.00 g, 12.0 mmol), Cul (65 mg, 0.33 mmol), and bis(triphenylphosphine)palladium)II)dichloride were suspended in degassed acetonitrile (MeCN) (5 mL) and degassed benzene (1 mL). The yellow suspension was sparged with argon for 30 min and degassed Et3N (1 mL) was added. The resulting brown suspension was sealed in a pressure vial, warmed to 80° C. and held there for 12 h. The mixture was then partitioned between EtOAc and KHSO4 solution. The organic layer was separated, washed with brine, dried MgSO4) and concentrated under reduced pressure. The dark yellow oil was purified by column chromatography on silica gel (25% Et2O in hexanes) to give 1.56 g (46%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563890B2
Source datasetuspto-grants-2009_07
ORD IDord-2fe543425c5d41608322a71ab1ccb910
Source noteuspto-grants-2009_07