Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Citric Acid | HCID 311 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Oxalic Acid | HCID 971 | — |
| Edukt | Phosphoric Acid | HCID 1004 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Methanesulfonic Acid | HCID 6395 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | Butyrate | HCID 104775 | — |
| Produkt | 1-Methoxypropan-2-yl 2-methylpropanoate | HCID 228677 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05426214 |
|---|
| Quelldatensatz | uspto-grants-1995_06 |
|---|
| ORD ID | ord-2292a2ddea45445f9e07397409476203 |
|---|
| Quellennotiz | uspto-grants-1995_06 |
|---|