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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427390Generated: October 31, 2026

1,2-Dichloroethane → (R)-2-Cyclohexylmethyl-4-morpholin-4-yl-4-oxo-butyric acid 1-methyl ester

https://huagongshe.com/reaction/427390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMorpholineHCID 8083—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(R)-2-(Cyclohexylmethyl)succinic acid-1-methyl esterHCID 2734511—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(R)-2-Cyclohexylmethyl-4-morpholin-4-yl-4-oxo-butyric acid 1-methyl esterHCID 5997294399%

Reaction Conditions

Temperature0 °C

Reaction Steps

(R)-2-(Cyclohexylmethyl)succinic acid 1-methyl ester (1.00 g, 4.38 mmol) was dissolved in 10 mL of DMF and cooled to 0° C. with an ice-water bath. EDC (1.12 g, 5.69 mmol) then 1-hydroxybenzotriazole (0.77 g, 5.69 mmol) were added and stirring continued, under argon, for 25 min. Morpholine (0.76 mL, 8.76 mmol) was added and stirring was continued overnight (16 h). The solution was diluted with 200 mL of EtOAc and washed with a 1.0 M solution of HCl (3×100 mL), a saturated solution of NaHCO3 (3×100 mL), water (100 mL), then with brine (100 mL). The organic layer was dried over MgSO4, filtered and concentrated by rotary evaporation to give (R)-2-Cyclohexylmethyl-4-morpholin-4-yl-4-oxo-butyric acid 1-methyl ester (1.26 g, 99%) as a white solid. The product was used in the following step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313117B1
Source datasetuspto-grants-2001_11
ORD IDord-ea565b3dd4d74af2a7168b3ca323d192
Source noteuspto-grants-2001_11