HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine hydrochloride → Ethyl 4'-(5-ethylaminopentyloxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4'-(5-bromopentyloxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate | HCID 66857022 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4'-(5-ethylaminopentyloxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate | HCID 11786051 | 64.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872026B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-88d1c2424e394d9fa8bf5430f3bade92 |
| Source note | uspto-grants-2011_01 |