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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253511Generated: October 27, 2026

Ethylamine hydrochloride → Ethyl 4'-(5-ethylaminopentyloxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate

https://huagongshe.com/reaction/253511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamine hydrochlorideHCID 11198—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4'-(5-bromopentyloxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylateHCID 66857022—
SolventEthanolHCID 702—
ProductEthyl 4'-(5-ethylaminopentyloxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylateHCID 1178605164.6%

Reaction Steps

In a manner similar to that of Example 1b, by reaction of 600 mg (1 mmol) of ethyl 4′-(5-bromopentyloxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate with 850 mg (10.4 mmol) of ethylamine hydrochloride and 1.44 g (10.4 mmol) of potassium carbonate in 50 ml of ethanol. 350 mg of ethyl 4′-(5-ethylaminopentyloxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate are obtained in the form of a colorless oil (yield=62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872026B2
Source datasetuspto-grants-2011_01
ORD IDord-88d1c2424e394d9fa8bf5430f3bade92
Source noteuspto-grants-2011_01