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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253484Generated: October 26, 2026

1,3-Dibromopropane → Ethyl 4'-(3-bromopropoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate

https://huagongshe.com/reaction/253484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4'-hydroxy-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylateHCID 57552328—
SolventMethyl Ethyl KetoneHCID 6569—
ProductEthyl 4'-(3-bromopropoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylateHCID 6685610755.5%

Reaction Steps

320 μl (3.14 mmol) of 1,3-dibromopropane and 440 mg (3.18 mmol) of potassium carbonate are added to a solution of 900 mg (2.1 mmol, 1 eq) of ethyl 4′-hydroxy-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate in 30 ml of methyl ethyl ketone. The reaction mixture is stirred overnight at room temperature and then for 1 day at reflux. The medium is cooled to room temperature and then filtered. The filtrate is evaporated and the residue is purified by chromatography on silica gel (eluent: 90/10 heptane/ethyl acetate). 640 mg of ethyl 4′-(3-bromopropoxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate are obtained in the form of a white solid (yield=55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872026B2
Source datasetuspto-grants-2011_01
ORD IDord-171ed02dcc294a2e9f0dbfa82aaf68ec
Source noteuspto-grants-2011_01