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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984995Generated: November 2, 2026

Carbon Dioxide → Sodium Salicylate

https://huagongshe.com/reaction/1984995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantPhenolHCID 996—
ReactantAspirinHCID 2244—
ReactantPhenolate SodiumHCID 4445035—
ReactantSodiumHCID 5360545—
ProductSodium SalicylateHCID 16760658—

Reaction Steps

Acetyl salicylic acid is commercially synthesized by Kolbe-Schmidt reaction which is a multi-step process. In this process, phenol is treated with a sodium base generating sodium phenoxide, which is then reacted with carbon dioxide under high temperature (125° C.) and pressure (100 atmosphere) to yield sodium salicylate, which on acidification yields salicylic acid. Salicylic acid is then acetylated with acetic anhydride to prepare acetyl salicylic acid. Existing process of the synthesis of acetyl salicylic acid is an acid catalyzed esterification reaction by the acetylation of the salicylic acid with acetic anhydride using conventional liquid acids, namely, conc. H2SO4 or conc. H3PO4 at the temperature of 80-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544831B2
Source datasetuspto-grants-2009_06
ORD IDord-071cbaf312b04836aee0d57a1f878051
Source noteuspto-grants-2009_06