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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327971Generated: October 30, 2026

Potassium Carbonate → HCID 67780109, compound

https://huagongshe.com/reaction/327971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
Reactant5-Oxo-2-(2-propenyl)-5,6,7,8-tetrahydro-1-naphthalenolHCID 19922106—
ReactantHCID 86747453HCID 86747453—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 67780109HCID 6778010996%

Reaction Steps

A mixture of 1.37 g (4 mmol) of (E)-3-[2-[[5-[(methylsulfonyl)oxy]pentyl]oxy]phenyl]-2-propenoic acid methyl ester from example 76, 0.81 g (4 mmol) of 5-oxo-2-(2-propenyl)-5,6,7,8-tetrahydro-1-naphthalenol, 0.8 g (5.8 mmol) of anhydrous, granular potassium carbonate, 0.08 mL of TDA-1, and 25 mL of toluene was stirred under reflux for 5.5 hr and at room temperature for 12 hr. After being treated with 0.3 g of additional potassium carbonate, the mixture was stirred and refluxed for a further 24 hr. The mixture was cooled and diluted with ether. The organic phase was washed with water and saturated brine and work-up was completed in the usual manner giving a brown oil. This material was chromatographed on 50 g of silica gel. Elution with 1:1 hexane-ether afforded 1.72 g (96%) of (E)-3-[2-[5-[(5-oxo-2-(2-propenyl)-5,6,7,8-tetrahydro-1-naphthalenyl)oxy]pentyloxy]phenyl]-2-propenoic acid methyl ester as a yellow-orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273999
Source datasetuspto-grants-1993_12
ORD IDord-7cef12d55cd345b48b20c32f9bd143d6
Source noteuspto-grants-1993_12