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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359616Generated: October 30, 2026

Acetaldehyde → HCID 14425602, compound

https://huagongshe.com/reaction/359616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantAcetonitrileHCID 6342—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 54481740HCID 54481740—
SolventAcetic AcidHCID 176—
ProductHCID 14425602HCID 14425602—

Reaction Steps

320 mg of p-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)propenyl]aniline are dissolved in 5 ml of acetonitrile and treated at room temperature with 440 mg of acetaldehyde and 190 mg of sodium cyanoborohydride. After 30 minutes the mixture is adjusted to a pH of 6-7 by the addition of acetic acid and 440 mg of acetaldehyde are again added thereto. After stirring at room temperature for 2 hours the reaction mixture is poured into ice-water, made alkaline by the addition of 2N potassium hydroxide solution and extracted with ether. The brownish oil obtained after drying and evaporation of the organic solvent is filtered over silica gel (elution agent hexane/ethyl acetate 9:1) and recrystallized from hexane. There are obtained 280 mg of N,N-diethyl-p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-propenyl]aniline in colourless crystals, melting point 89°-90°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001276
Source datasetuspto-grants-1991_03
ORD IDord-e33f76db79e64cc284bb8b7482fa96df
Source noteuspto-grants-1991_03