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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720295Generated: November 2, 2026

Sodium Iodide → 1-(Anilinocarbonylmethyl)-4-methoxymethoxypiperidine

https://huagongshe.com/reaction/1720295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantChloroacetanilideHCID 11485—
ReactantHCID 15172750HCID 15172750—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-(Anilinocarbonylmethyl)-4-methoxymethoxypiperidineHCID 2292368890.5%

Reaction Steps

1.7 ml of chloroacetyl chloride was dropwise added to a solution of 3.0 g of aniline hydrochloride and 7 ml of triethylamine in 30 ml of dichloromethane. The mixture was stirred at room temperature for 3 hours, then washed with water and a saturated aqueous sodium hydrogencarbonate solution in this order, and dried with magnesium sulfate. The solvent was removed by distillation. The resulting residue was crystallized from ethyl acetate-n-hexane to obtain 2.45 g of N-(2-chloroacetyl)aniline as a light brown solid. A suspension of 2.45 g of the N-(2-chloroacetyl)-aniline, 2.8 g of 4-methoxymethoxypiperidine, 2.45 g of sodium iodide and 2.3 ml of triethylamine dissolved in 30 ml of acetonitrile was refluxed for 1.5 hours. The reaction mixture was diluted with ethyl acetate. The dilution was washed with water and dried with magnesium sulfate. The solvent was removed by distillation. The resulting residue was purified by a silica gel column chromatography (eluant: ethyl acetate: n-hexane=1:1) to obtain 3.64 g of 1-(anilinocarbonylmethyl)-4-methoxymethoxypiperidine as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506239
Source datasetuspto-grants-1996_04
ORD IDord-7d564b8496cb4692a2fd5a5f4b890779
Source noteuspto-grants-1996_04