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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253486Generated: October 30, 2026

Water → Ethyl 4'-(3-isopropylaminopropoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate

https://huagongshe.com/reaction/253486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsopropylamineHCID 6363—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4'-(3-iodopropoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylateHCID 66856963—
SolventAcetonitrileHCID 6342—
ProductEthyl 4'-(3-isopropylaminopropoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylateHCID 1142116830.3%

Reaction Steps

430 μl (5 mmol) of isopropylamine and 420 mg (3 mmol) of potassium carbonate are added to a solution of 600 mg (1 mmol) of ethyl 4′-(3-iodopropoxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate in 50 ml of acetonitrile. The reaction mixture is stirred at reflux overnight. The reaction is stopped by adding water and is then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then purified by chromatography on silica gel (50/50 heptane/ethyl acetate). 160 mg of ethyl 4′-(3-isopropylaminopropoxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate are obtained in the form of a yellowish solid (m.p.=171° C., yield=30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872026B2
Source datasetuspto-grants-2011_01
ORD IDord-80cee948fd0b462da4e4e62f084e01f9
Source noteuspto-grants-2011_01