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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340771Generated: October 25, 2026

1,2-Dichloroethane → Benzyl 3-oxocyclohexanecarboxylate

https://huagongshe.com/reaction/340771

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzyl AlcoholHCID 244—
Reactant3-Oxocyclohexane-1-carboxylic acidHCID 2760252—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-oxocyclohexanecarboxylateHCID 58964377—

Reaction Steps

To a solution of 3-oxocyclohexane carboxylic acid (1.5 g, 10.6 mmol) in CH2Cl2 (35 mL) were added DMAP (0.129 g, 1.06 mmol), EDC (4.05 g, 21.1 mmol), and BnOH (1.2 mL, 11.6 mmol). The reaction was maintained at ambient temperature for 1 h. The reaction was further diluted with CH2Cl2, and then washed with saturated aqueous NaHCO3, followed by brine. The organic layer was separated, dried with MgSO4, filtered, and concentrated. The resulting crude product was used in the next step without further purification. LCMS: calculated for C14H16O3 232.28, observed m/e 233.1 (M+H)+ 255.0 (M+Na) (Rt 1.74/4 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895596B2
Source datasetuspto-grants-2014_11
ORD IDord-600420e4e06b4ac9b8846904f3bc01a7
Source noteuspto-grants-2014_11