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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253150Generated: October 25, 2026

Phosgene → Benzyl 4-(3,3-dimethylpiperidine-1-carbonyl)morpholine-2-carboxylate

https://huagongshe.com/reaction/253150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactant3,3-DimethylpiperidineHCID 70942—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl morpholine-2-carboxylateHCID 58367827—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-(3,3-dimethylpiperidine-1-carbonyl)morpholine-2-carboxylateHCID 66844830—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a dry 25-mL RBF, phosgene (0.25 ml, 0.47 mmol) was dissolved in DCM (2 mL) and the solution was cooled to 0° C. A solution of benzyl morpholine-2-carboxylate (50%, 0.070 g, 0.16 mmol, Example 458, Step 2) and N-ethyl-N-isopropylpropan-2-amine (0.041 ml, 0.24 mmol) in DCM (2 mL) was added. The solution was stirred at 0° C. for 4 h, and the ice bath was removed, and the mixture stirred at RT for 1 hour. The reaction mixture was concentrated, and the residue dissolved in DCM (2 mL), and N-ethyl-N -isopropylpropan-2-amine (0.041 ml, 0.24 mmol) and 3,3-dimethylpiperidine (0.022 g, 0.20 mmol) were added by syringe. After 14 h, the reaction mixture was concentrated. The residue was purified through silica gel (20 mL) using 50% EtOAc-hexane to afford the title compound. MS m/z 361 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872009B2
Source datasetuspto-grants-2011_01
ORD IDord-54b563972a91413ab69b8cb895abe413
Source noteuspto-grants-2011_01