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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892272Generated: October 29, 2026

Tetrahydrofuran → HCID 23600742, compound

https://huagongshe.com/reaction/892272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant2-Methoxybenzoyl chlorideHCID 88969—
ReactantHCID 23600788HCID 23600788—
ProductHCID 23600742HCID 23600742—

Reaction Steps

A solution of compound 2 (0.03 g; 0.009 mmol) in tetrahydrofuran (2 mL) was treated with triethylamine (0.1 mL; 0.7 mmol) and o-anisoyl chloride (0.05 g; 0.3 mmol) at room temperature. After stirring 15 h the tetrahydrofuran was removed by evaporation and the residue was purified by prep LC to give 0.011 g of compound 4-(2-methoxy-benzoylamino)-4-phenyl-piperidine-1-carboxylic acid benzyl ester as a white solid. LCMS m/z=461 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005436B2
Source datasetuspto-grants-2006_02
ORD IDord-7748ab4be5084949812bebfc91a6d8d3
Source noteuspto-grants-2006_02