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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796136Generated: October 29, 2026

Diisopropylamine → (R)-2-(1-Benzyl-cyclopropylmethyl)-4-morpholin-4-yl-4-oxo-butyric acid

https://huagongshe.com/reaction/1796136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantMorpholineHCID 8083—
ReactantPyBOPHCID 2724699—
Reactant(R)-2-(1-Benzyl-cyclopropylmethyl)-succinic acid 1-methyl esterHCID 69619387—
SolventDichloromethaneHCID 6344—
Product(R)-2-(1-Benzyl-cyclopropylmethyl)-4-morpholin-4-yl-4-oxo-butyric acidHCID 58619525—

Reaction Steps

To a solution of (R)-2-(1-Benzyl-cyclopropylmethyl)-succinic acid 1-methyl ester (2.453 g, 8.88 mmol), di-isopropyl amine (1.1 eq, 9.76 mmol, 1.26 g) and morpholine (1.5 eq., 13.3 mmol, 1.16 g) in dry dichloromethane under N2 was added PyBOP (1.1 eq., 9.76 mmol, 5.08 g). The mixture was stirred at room temperature for 5 hr, and concentrated in vacuum. The residue was dissolved in ethyl acetate (150 mL) and washed with water (100 mL), NH4Cl (100 mL), NaHCO3 (2×100 mL), then water (100 mL). The organic layer was dried (MgSO4) and concentrated in vacuum. The residue was purified over 120 g silica gel, eluted with ethyl acetate:heptane (1:1.5, 1:1, to 2:1) to afford the desired compound contaminated with PyBOP residues. A solution of the mixture in ether containing ethyl acetate (250 mL total) was washed with dilute HCl (150 mL), water (150 mL) dilute NaOH (150 mL) then water (150 mL). The organic layer was dried (MgSO4) and concentrated in vacuum to afford (R)-2-(1-Benzyl-cyclopropylmethyl)-4-morpholin-4-yl-4-oxo-butyric acid methyl ester as a white solid (2.292 g, 74.7% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030116B2
Source datasetuspto-grants-2006_04
ORD IDord-c320e4ad85e84d76bcb1d4ff63042840
Source noteuspto-grants-2006_04