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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586633Generated: November 2, 2026

(Methylsulfonyl)acetonitrile → HCID 67639908, compound

https://huagongshe.com/reaction/1586633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Methylsulfonyl)acetonitrileHCID 75283—
Reactant4-(2-hydroxyethoxy)-3-methoxybenzaldehydeHCID 3152712—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 67639908HCID 67639908—

Reaction Steps

A mixture of 4-(2-hydroxyethoxy)-3-methoxybenzaldehyde (0.98 g, 0.005 mol), (see Example 1 of U.S. Pat. No. 4,707,537, supra), methylsulfonylacetonitrile (0.60 g, 0.005 m), ethanol (10 mL) and piperidine (5 drops) is heated at reflux for 1 hour, during which time the product crystallizes. The reaction mixture is allowed to cool and the very pale yellow product is collected by filtration, washed with ethanol and dried in air. The yield of product is 1.05 g (70.9%). Mass spectrometry supports the following structure: ##STR22## In methylene chloride the product has an absorption maximum at 362 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215876
Source datasetuspto-grants-1993_06
ORD IDord-ada37b2f74a24a89a75c5cc1e926bff0
Source noteuspto-grants-1993_06