HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Methyl Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Methyl Acetate | HCID 6584 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Rhodium chloride trihydrate | HCID 11459718 | — |
| Product | Methyl Acetate | HCID 6584 | — |
| Product | Methyl formate | HCID 7865 | — |
Reaction Steps
0.34 g of rhodium chloride trihydrate, 4.9 ml of methyl iodide, 0.6 g of aluminum powder, 27 g (587 mmol) of formic acid and 41 g (553 mmol) of methyl acetate were fed into the same autoclave as the one used in Example 1, followed by pressurizing by carbon monoxide to 20 kg/cm2 in the same manner as described in Example 2. The reaction was carried out at 170° C. for 30 minutes. 31 mmol of methyl formate, 72 mmol of methyl acetate and 931 mmol of acetic acid were produced. This means that 81.4 molar % of the amount of the methyl ester moiety contained in the raw material was converted into an acetyl group, corresponding to an acetylation rate of 13.0 mol/l.hr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04996357 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-2aaa2ea8fc8b4295b48548847f5246f8 |
| Source note | uspto-grants-1991_02 |