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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893071Generated: October 25, 2026

Dimethylacetamide → 4-{4-[2-(4-Pentyl-cyclohexyl)-ethenyl]-phenyl}cyclohexane carboxylic acid methyl ester

https://huagongshe.com/reaction/1893071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Pentyl-4-vinyl-cyclohexaneHCID 19039193—
Reactant4-(4-Bromophenyl)cyclohexane carboxylic acid methyl esterHCID 58453203—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product4-{4-[2-(4-Pentyl-cyclohexyl)-ethenyl]-phenyl}cyclohexane carboxylic acid methyl esterHCID 5845321762%

Reaction Steps

180 mL of N,N-dimethylacetamide (DMA) solution including 12.8 g (60.1 mmol) of potassium phosphate, 14.3 g (48 mmol) of 4-(4-bromophenyl)cyclohexanecarboxylic acid methyl ester produced in Example 1-1, and 8.33 g (40 mmol) of 1-pentyl-4-vinyl-cyclohexane was poured to flask filled with Argon gas. Then, 0.17 g (catalytic amount) of palladium acetate was added to the flask and reacted in oil bath at 120° C. for 32 hours. After reaction, 100 mL of distilled water was added to the reaction mixture, extracted by ethyl acetate, and then the aqueous layer was extracted by chloroform. The organic layer was dried by Na2SO4, concentrated under reduced pressure, and then recrystallized from ethanol to obtain 9.8 g (62%) of 4-{4-[2-(4-pentyl-cyclohexyl)-ethenyl]-phenyl}cyclohexane carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08512598B2
Source datasetuspto-grants-2013_08
ORD IDord-14f5fc01f0c14d63b8ea886b39ed57ed
Source noteuspto-grants-2013_08