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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353468Generated: October 27, 2026

Hydrochloric Acid → 1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid

https://huagongshe.com/reaction/353468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyclohexanecarboxylic acidHCID 7413—
ReactantSodium hydrideHCID 24758—
ReactantPentane, 3-(bromomethyl)-HCID 77432—
ReactantLithium isopropylamideHCID 10877046—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
Product1-(2-Ethyl-butyl)-cyclohexanecarboxylic acidHCID 1048875164%

Reaction Steps

A suspension of 60% sodium hydride (980 mg) in tetrahydrofuran (80 ml) was stirred at room temperature and a tetrahydrofuran solution (10 ml) containing cyclohexanecarboxylic acid (3.00 g) was added dropwise thereto. After completion of addition, a mixture was stirred for 1 hour and cooled to 0° C., followed by adding a cyclohexane solution (18.7 ml) containing 1.5 M lithium isopropylamide dropwise thereto. Then, after stirring at room temperature for 1.5 hours and cooling to 0° C., a tetrahydrofuran solution (10 ml) containing 1-bromo-2-ethylbutane (4.64 g) was added dropwise thereto. The solution was gradually warmed to room temperature and stirred overnight. Water and a 10% hydrochloride solution were added to this reaction solution and the solution was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. After drying, the resulting solution was concentrated to obtain 1-(2-ethylbutyl)cyclohexanecarboxylic acid (3.17 g, yield: 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753346B2
Source datasetuspto-grants-2004_06
ORD IDord-ce1d467411124cf3b5a5d1ccaa53df3b
Source noteuspto-grants-2004_06