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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045054Generated: November 3, 2026

Iodoethane → HCID 67044939, compound

https://huagongshe.com/reaction/1045054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 11019548HCID 11019548—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67044939HCID 6704493978.5%

Reaction Steps

4-Isopropyl-cyclohexanecarboxylic acid methyl ester (1.1 g, 6 mmol) was alkylated using a method analogous to General Procedure F using LDA (9 mmol) and iodoethane (1.4 g, 9 mmol) in THF (20 mL) at −78° C. to RT to produce 1-ethyl-4-isopropyl-cyclohexanecarboxylic acid methyl ester (1.0 g, 78% yield) as a mixture of isomers. Hydrolysis of this ester using KOH (12.5 mmol) in aqueous EtOH (1:1; 5 mL) at 150° C. for 2 hr in a pressurized vessel following a microwave method analogous to General Procedure G2 gave 1-ethyl-4-isopropyl-cyclohexanecarboxylic acid (800 mg, 86% yield) as a mixture of isomers after workup by evaporation of the solvent, treatment with aq 2 N HCl, extractive workup, and evaporation of the solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563742B2
Source datasetuspto-grants-2013_10
ORD IDord-d2f994a44e734a8b95135de81ddce57b
Source noteuspto-grants-2013_10