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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905554Generated: October 29, 2026

Acetaldehyde → Methyl Acetate

https://huagongshe.com/reaction/1905554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantMethanolHCID 887—
ReactantMethyl AcetateHCID 6584—
ReactantAcetic AnhydrideHCID 7918—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductMethyl AcetateHCID 6584—
ProductVinyl AcetateHCID 7904—

Reaction Steps

Therefore, in step (a) of the process of this invention, methanol is hydrocarbonylated to C2 compounds such as ethanol, acetaldehyde, methyl acetate and dimethylacetal, and the reaction mixture containing these compounds is then freed of ethanol, acetaldehyde, methyl acetate and dimethylacetal; concurrently, in step (b), methyl acetate is carbonylated to acetic anhydride which is then freed from the reaction mixture; the mixture of acetaldehyde and dimethylacetal separated in step (a) is reacted with acetic anhydride to form a vinyl acetate precursor ethylidene diacetate (hereunder referred to as ED) and methyl acetate (step (c)), or vinyl acetate, acetic acid and methyl acetate are produced directly and simultaneously (step (c) combined with step (d)); both the methyl acetate produced in the step (c) or the combination of steps (c) and (d) and the methyl acetate produced in the step (a) are carbonylated to acetic anhydride. The above cycle is repeated. When ED is synthesized as a precursor, it is thermally decomposed (step (d)) to vinyl acetate and acetic acid. In summary, this invention accomplishes simultaneous production of vinyl acetate, acetic acid and ethanol from methanol, carbon monoxide and hydrogen.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04843170
Source datasetuspto-grants-1989_06
ORD IDord-b2c9a2b6ac0342cc97a40e3d3b7d3749
Source noteuspto-grants-1989_06