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HRID 22083作成日:2026年10月25日

Citric Acid → Butyrate

https://huagongshe.com/reaction/22083

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物Hydrochloric AcidHCID 313—
反応物Oxalic AcidHCID 971—
反応物Phosphoric AcidHCID 1004—
反応物Sulfuric AcidHCID 1118—
反応物p-Toluenesulfonic acidHCID 6101—
反応物Methanesulfonic AcidHCID 6395—
溶媒Acetic AcidHCID 176—
生成物ButyrateHCID 104775—
生成物1-Methoxypropan-2-yl 2-methylpropanoateHCID 228677—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426214
出典データセットuspto-grants-1995_06
ORD IDord-2292a2ddea45445f9e07397409476203
出典メモuspto-grants-1995_06