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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641757Generated: November 3, 2026

Formaldehyde → HCID 57736420, compound

https://huagongshe.com/reaction/1641757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 57736466HCID 57736466—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 57736420HCID 5773642056%

Reaction Steps

To a solution of 5-[[(4-chlorophenyl)sulfonyl](2,3,6-trifluorophenyl)methyl]-4-methylpyridine-2-carboxamide (190 mg, 0.418 mmol) in ethylene glycol dimethyl ether (4 ml), an aqueous solution of formaldehyde (37%, 94.2 μl) and 1 N aqueous sodium hydroxide (21.0 μl) were added at room temperature, and the mixture was stirred for 17 hours. Ethyl acetate was added to the reaction mixture, and the mixture was washed with saturated aqueous ammonium chloride. Subsequently, 1 N hydrochloric acid was added to the organic layer, and the mixture was stirred for 1 hour. After the organic layer was separated, the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtered, and then the filtrate was concentrated under reduced pressure. The resulting residue was subjected to flash silica gel chromatography, and the fraction obtained from an elution with hexane:ethyl acetate=1:1 was concentrated under reduced pressure. The resulting residue was washed with a mixed solvent of ethyl acetate and diethyl ether, and then was collected by filtration, to obtain the title compound (113 mg, 0.233 mmol, 56%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114886B2
Source datasetuspto-grants-2012_02
ORD IDord-9cf9f87f3f544929bc1dc80ad4ee26c0
Source noteuspto-grants-2012_02