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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614632Generated: October 31, 2026

Benzoyl chloride → 1-Benzoyl-N,alpha-bis(4-fluorophenyl)-4-piperidinemethanamine

https://huagongshe.com/reaction/1614632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantN,alpha-bis(4-fluorophenyl)-4-piperidinemethanamineHCID 19771957—
SolventDichloromethaneHCID 6344—
Product1-Benzoyl-N,alpha-bis(4-fluorophenyl)-4-piperidinemethanamineHCID 19771949—

Reaction Steps

A solution of N,α-bis(4-fluorophenyl)-4-piperidinemethanamine (3.21 g, 0.0106 mol), triethylamine (2.5 g, 0.025 mol), and benzoyl chloride (1.70 g, 0.012 mol) in 400 mL of methylene chloride was stirred 16 h at room temperature. The reaction was concentrated to dryness and dissolved in chloroform. The chloroform layer was extracted successively with water, 1N sulfuric acid, and 5% sodium hydroxide. The chloroform layer was dried (Na2SO4) and filtered. The chloroform was removed to give a fluffy-white residue. This material was dissolved in methylene chloride and chromatographed by flash chromatography on silica gel. Elution was accomplished using methylene chloride, 1% acetone-methylene chloride, 2% acetone-methylene chloride, and 4% acetone-methylene chloride. Fractions of similar purity were combined, and solvents removed to give a fluffy-white residue. This material was triturated with isopropyl ether and chilled in a freezer. A white solid was isolated and dried, 16 h at 78° C. This furnished 1.40 g (32.5%) of white crystalline solid, mp 157°-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198449
Source datasetuspto-grants-1993_03
ORD IDord-a917f4ce311d4b919fba4ffe41a4c87b
Source noteuspto-grants-1993_03