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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386324Generated: October 26, 2026

Water → 4'-Pentyl-bicyclohexyl-4-carboxylic acid 6-(2-methyl-acryloyloxy)-hexyl ester

https://huagongshe.com/reaction/386324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethacrylic AcidHCID 4093—
ReactantSodium hydrideHCID 24758—
Reactant4'-Pentyl-bicyclohexyl-4-carboxylic acid 6-bromo-hexyl esterHCID 59289042—
SolventDimethylformamideHCID 6228—
Product4'-Pentyl-bicyclohexyl-4-carboxylic acid 6-(2-methyl-acryloyloxy)-hexyl esterHCID 59289040—

Reaction Steps

A solution of methacrylic acid (3.6 g, 41.8 mmol) in dimethylformamide (30 ml) is added dropwise to an ice cooled slurry of sodium hydride (60% suspension in paraffin oil) (1.5 g, 37.5 mmol) in dimethylformamide (50 ml). Once addition is complete, the mixture is allowed to warm to room temperature and is stirred for 1 h, the intermediate 4′-pentyl-bicyclohexyl-4-carboxylic acid 6-bromo-hexyl ester (15.0 g, 33.8 mmol) in dimethylformamide (100 ml) is added dropwise. The mixture is stirred at 50° C. over night. The mixture is cooled to room temperature, poured into icy water, and this is extracted three times with DCM. The DCM solution is washed with brine, water and then dried over sodium sulphate. The solution is evaporated to dryness and recrystallised from acetonitrile to afford a white waxy solid. Further purification is achieved by preparative HPLC using water/acetonitrile as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372307B2
Source datasetuspto-grants-2013_02
ORD IDord-20399f3c8b2b4a9d9914604b169a4c07
Source noteuspto-grants-2013_02