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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427466Generated: November 1, 2026

Hydrochloric Acid → 1-Cyanomethyl-cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/reaction/2427466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromoacetonitrileHCID 11534—
ReactantMethyl cyclohexanecarboxylateHCID 20748—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTetrahydrofuran heptane ethylbenzolHCID 22742125—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-Cyanomethyl-cyclohexanecarboxylic acid methyl esterHCID 5765780841%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Treat a −78° C. solution of methyl cyclohexane carboxylate (15.0 g, 0.105 mol) in THF (150 mL) with a 2M solution of lithium diisopropylamide in heptane/THF/ethylbenzene (63.3 mL, 0.126 mol) and stir at −78° C. for 20 minutes under N2. Treat the reaction with bromoacetonitrile (25.31 g, 0.211 mol) and stir at −78° C. for 15 minutes. Warm the reaction to room temperature and stir 4 hours. Acidify the reaction with 1 N HCl and then dilute the reaction with ethyl acetate and wash with water. Dry the organic layer (Na2SO4) and remove the solvent in vacuo to afford crude product. Purify with a 0 to 30% ethyl acetate in hexanes gradient on silica gel to afford 7.78 g (41%) of the titled product. Rf=0.32 (3/1 hexanes/ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968585B2
Source datasetuspto-grants-2011_06
ORD IDord-fa5e979fc0fc468c9726504a37d7b17b
Source noteuspto-grants-2011_06