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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907741Generated: October 25, 2026

1,2-Dichloroethane → Tert-butyl 4-(3-oxopyrrolidin-1-yl)benzoate

https://huagongshe.com/reaction/1907741

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMethyl morpholine oxideHCID 82029—
ReactantTert-butyl 4-(3-hydroxypyrrolidin-1-yl)benzoateHCID 10084125—
CatalystHCID 178419074HCID 178419074—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(3-oxopyrrolidin-1-yl)benzoateHCID 1001551729%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of alcohol 266 (2.75 g, 10.45 mmol), NMO (5.8 g, 49 mmol) and 4 Å molecular sieves (8.34 g) was suspended in dry DCM (100 mL) and dry 1,2-dichloroethane (100 mL), stirred at room temperature for 45 min, and then cooled to 0° C. for the addition of solid TPAP (0.36 g, 1.03 mmol). The reaction mixture was stirred at 0° C. for 30 min and then at room temperature for 5 h, filtered through Celite®/silica gel using 50% AcOEt in hexanes as an eluent, then concentrated. The residue was purified by flash chromatography (eluent: 30% to 50% AcOEt in hexane) to provide title compound 267 (0.78 g, 29% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598168B2
Source datasetuspto-grants-2013_12
ORD IDord-7669fc4976394115afbe12a321938740
Source noteuspto-grants-2013_12