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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732444Generated: October 31, 2026

4-Aminobenzaldehyde → HCID 54203179, compound

https://huagongshe.com/reaction/1732444

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzaldehydeHCID 11158—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl (methylsulfinyl)methyl sulfideHCID 99129—
ProductHCID 54203179HCID 5420317962.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

Flakes of sodium hydroxide (55 mg) were added to a mixture of 201 mg of p-aminobenzaldehyde and 798 mg of FAMSO, and the mixture was stirred at 80° C. for 30 minutes. After adding 50 ml of a saturated aqueous solution of ammonium chloride, the reaction mixture was extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was chromatographed on a silica gel column using methylene chloride as an eluant to afford oil-containing orange crystals. Washing of the crystals with acetone afforded 235 mg of 1-methylsulfinyl-1-methylthio-2-(p-aminophenyl)ethylene as pale yellow crystals in a yield of 62%. Samples for analysis were obtained as colorless crystals by recrystallization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237298
Source datasetuspto-grants-1980_12
ORD IDord-a4329f82d3464d909fd89bda2295a09c
Source noteuspto-grants-1980_12