Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667572Generated: October 29, 2026

Acetaldehyde → Glyoxylic Acid

https://huagongshe.com/reaction/1667572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantAmmoniaHCID 222—
ReactantFormaldehydeHCID 712—
ReactantNitric AcidHCID 944—
ReactantPyridineHCID 1049—
ReactantPeracetic AcidHCID 6585—
ProductGlyoxylic AcidHCID 760—
Product5-Ethyl-2-methylpyridineHCID 7728—
ProductGlyoxalHCID 7860—

Reaction Steps

A considerable proportion of acetaldehyde is used for the preparation of acetic esters. For example, ethyl acetate is prepared in a rearrangement reaction with aluminium alcoholates as a catalyst (Claisen-Ti{hacek over (s)}{hacek over (c)}enko reaction). A substantial proportion is also used with formaldehyde for the production of pentaerythritol, an intermediate in the production of alkyl resins and plasticizers and emulsifiers. Furthermore, acetaldehyde is an intermediate in the preparation of butadiene starting from acetylene via acetaldol and its hydration product 1,3-butanediol. The formation of the acetaldol, which can be dehydrated to give crotonaldehyde, takes place by aldol addition of acetaldehyde. The reaction of acetaldehyde with nitrogen compounds to give pyridine and derivatives thereof is becoming increasingly important. Thus, 5-ethyl-2-methylpyridine is prepared in a liquid-phase reaction from acetaldehyde and ammonia. Addition of formaldehyde or acrolein leads to the formation of pyridine and alkylpyridines. Acetaldehyde is further used in the production of peracetic acid, in the oxidation with nitric acid to give glyoxal or glyoxalic acid and in the addition reactions with hydrocyanic acid to give lactonitrile, a precursor of acrylonitrile, and acetic anhydride to give ethylidene diacetate, an intermediate in the vinyl acetate process [Eck2007].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044246B2
Source datasetuspto-grants-2011_10
ORD IDord-631fb0fda9524282b766933df5679e0f
Source noteuspto-grants-2011_10