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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275499Generated: November 2, 2026

Triethylamine → HCID 22619434, compound

https://huagongshe.com/reaction/1275499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 4-iodosalicylateHCID 11380407—
ReactantHCID 22619460HCID 22619460—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 22619434HCID 22619434—

Reaction Steps

2.5 g (10.8 mmol) of α-ethynyl-4,4-dimethyl-7-thiochromanmethanol, 3 g (10.8 mmol) of methyl 2-hydroxy-4-iodobenzoate and 50 ml of triethylamine were introduced into a three-necked flask. The reaction mixture was degassed with nitrogen for 30 min. and then 600 mg (0.86 mmol) of bis(triphenylphosphine)palladium(II) chloride and 240 mg (1.3 mmol) of copper iodide were successively added. Stirring was carried out at room temperature for four hours and the reaction mixture was evaporated to dryness and the residue obtained 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 dichloromethane. 3.2 g (80%) of methyl 2-hydroxy-4-[3-hydroxy-3-(4,4-dimethylthiochroman-7-yl)-1-propynyl]benzoate, with a melting point of 101°-102° C., were recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162445
Source datasetuspto-grants-2000_12
ORD IDord-9f744ad8c94049e194835bd6c524cd86
Source noteuspto-grants-2000_12