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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275502Generated: November 3, 2026

Triethylamine → HCID 22619447, compound

https://huagongshe.com/reaction/1275502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant4-BromobenzaldehydeHCID 70741—
Reactantalpha-Ethynyl-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenemethanolHCID 11817362—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 22619447HCID 22619447—

Reaction Steps

2.42 g (10 mmol) of α-ethynyl-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenemethanol, 2 g (11 mmol) of 4-bromobenzaldehyde and 50 ml of triethylamine were introduced into a three-necked flask. The reaction mixture was degassed with nitrogen for 30 min. and then 169 mg (0.75 mmol) of palladium(II) acetate and 393 mg (1.5 mmol) of triphenylphosphine were successively added. Heating was carried out at 60° C. for one hour, the reaction mixture was evaporated to dryness and the residue obtained was taken up in water and ethyl ether. The organic phase was separated by settling, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a silica column eluted with a mixture of dichloromethane and heptane (70/30). 1.23 g (35.5%) of 4-(3-hydroxy-3-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propynyl]benzaldehyde, with a melting point of 104°-105° C., was recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162445
Source datasetuspto-grants-2000_12
ORD IDord-eea60e5044e748fea89f6a2cd9fcd777
Source noteuspto-grants-2000_12