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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22083Generated: October 25, 2026

Citric Acid → Butyrate

https://huagongshe.com/reaction/22083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantHydrochloric AcidHCID 313—
ReactantOxalic AcidHCID 971—
ReactantPhosphoric AcidHCID 1004—
ReactantSulfuric AcidHCID 1118—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantMethanesulfonic AcidHCID 6395—
SolventAcetic AcidHCID 176—
ProductButyrateHCID 104775—
Product1-Methoxypropan-2-yl 2-methylpropanoateHCID 228677—

Reaction Steps

The catalysts used in the present invention include inorganic acids, such as sulfuric acid, hydrochloric acid and phosphoric acid, and organic acids, such as acetic acid, oxalic acid, citric acid, p-toluene sulfonic acid and methane sulfonic acid, among which the strong acids including sulfuric acid, p-toluene sulfonic acid and methane sulfonic acid are preferred. The boiling points of propylene glycol monomethyl ether iso-butyrate and n-butyrate obtained according to the present application are 167.2° C. and 180.5° C., respectively, while other reactants and products having respective boiling point of 120° C. for PGM, 154.4° C. for iso-butyric acid, 164° C. for n-butyric acid and 100° C. for water. It is apparently easier to rectify this solution comparing the respective boiling point of 146° C. for propylene glycol monomethyl ether acetate, 118° C. for acetic acid and 120° C. for PGM as in the conventional case. This is one of the effect achieved by the process according to the present invention.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426214
Source datasetuspto-grants-1995_06
ORD IDord-2292a2ddea45445f9e07397409476203
Source noteuspto-grants-1995_06