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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913214Generated: November 1, 2026

Ethyl Acetate → HCID 66879199, compound

https://huagongshe.com/reaction/1913214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-CarboxyMethyl-cyclohexanecarboxylic acid ethyl esterHCID 15896192—
ReactantHCID 66896914HCID 66896914—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66879199HCID 66879199—

Reaction Steps

To a 100 mL round-bottom vessel was charged 2-(4-(ethoxycarbonyl)cyclohexyl)acetic acid (Int-4c, 4.03 g, 18.79 mmol) and THF (20 mL). To this solution was added N,N′-carbonyldiimidazole (3.66 g, 22.55 mmol). The resulting solution was allowed to stir 18 hours at room temperature. After 18 hours, in a separate 250 mL round-bottom vessel, 80 mL THF was added and the flask was flushed with argon. This solution was cooled to −78° C. in dry ice/IPA bath. To this solution was added LiHMDS (1.0 M in THF, 39.46 mmol, 39.46 mL). To the resulting solution was added dropwise dry EtOAc (40.4 mmol, 3.95 mL). This solution was allowed to stir at −78° C. for one hour. After one hour, the solution of crude ethyl 4-(2-(1H-imidazol-1-yl)-2-oxoethyl)cyclohexanecarboxylate (Int-4d) in THF was added dropwise. This solution was allowed to gradually warm to room temperature and the reaction was stirred overnight. After 18 hours, the reaction was quenched with saturated NH4Cl(aq) and extracted with Et2O (x3). The combined organics were dried over Na2SO4 and the residue was purified via silica gel chromatography to yield the title compound as clear oil. Yield=2.33 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609675B2
Source datasetuspto-grants-2013_12
ORD IDord-60a37e04966a471db408396bfd7255bb
Source noteuspto-grants-2013_12