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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961629Generated: October 31, 2026

4-(4-Fluorobenzoyl)piperidine → HCID 66626278, compound

https://huagongshe.com/reaction/1961629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Fluorobenzoyl)piperidineHCID 2724440—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 45091916HCID 45091916—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 66626278HCID 6662627861.7%

Reaction Steps

A mixture of 4-(4-fluorobenzoyl)piperidine (0.300 g, 1.2 mmol), Trans-(2-Formyl-cyclopropylmethyl)-carbamic acid tert-butyl ester (0.294 g, 1.2 mmol), in 1, 2 dichloroethane (2 mL) was stirred for 4 h at room temperature and sodium triacetoxyborohydride (0.470 g, 2.2 mmol) was added and the resulting solution was stirred for 12 hours until the TLC indicated completion of the reaction. The mixture was filtrated and concentrated to dryness and purified with column chromatography on silica gel using CH2Cl2-CH2Cl2/MeOH (1-9:1). The product fractions were concentrated to give 0.288 g (0.74 mmol, 60% yield) of a white solid. MS (m/e): 391.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415350B2
Source datasetuspto-grants-2013_04
ORD IDord-e78412ec32cf441fa8c0f248dd371854
Source noteuspto-grants-2013_04