HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253491Generated: October 25, 2026
Water → Ethyl 4'-(3-dimethylaminopropoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate
https://huagongshe.com/reaction/253491
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Dimethylamino)propyl chloride hydrochloride | HCID 94308 | — |
| Reactant | Ethyl 4'-hydroxy-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate | HCID 57552328 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 4'-(3-dimethylaminopropoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate | HCID 11306847 | 81.9% |
Reaction Steps
440 mg (2.78 mmol) of 3-dimethylaminopropyl chloride hydrochloride and 970 mg (7 mmol) of potassium carbonate are added to a solution of 1 g (2.33 mmol) of ethyl 4′-hydroxy-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate in 50 ml of acetone. The reaction mixture is stirred for 48 hours at reflux. 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 (eluent: 90/10 ethyl acetate/methanol). 980 mg of ethyl 4′-(3-dimethylaminopropoxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate are obtained in the form of a yellow oil (yield=82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07872026B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-8b56a52b6a194f9e96cb35afea889f17 |
|---|
| Source note | uspto-grants-2011_01 |
|---|