HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483267Generated: October 25, 2026
Acetic Acid → 2-Propenoic acid, 3-phenyl-, methyl ester
https://huagongshe.com/reaction/483267
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Barium(2+) dichloride | HCID 5360350 | — |
| Reactant | HCID 178514649 | HCID 178514649 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 2-Propenoic acid, 3-phenyl-, methyl ester | HCID 7644 | — |
Reaction Steps
Into the same autoclave as that used in Example 4 were charged 2% Pd/A.C. in an amount of 0.5 mmol as Pd, 20 mmol of cupric acetate, 20 mmol of barium chloride, 160 mmol of acetic acid, 70 ml of styrene and 30 ml of methanol, then, a mixed gas of nitrogen/oxygen/carbon monoxide (86.0/5.5/8.5 in volume ratio) was introduced to make the pressure inside the reaction system 20.0 kg/cm2G, and while maintaining this pressure and passing the mixed gas at a gas flow rate at the reactor outlet of 76.6 Nl/hr, the reaction was effected for 1.5 hours while maintaining the reaction temperature at 120° C. The amounts of methyl cinnamate formed at intervals are shown in FIG. 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04578507 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-0597029dcc104b34834dde8183b5b529 |
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| Source note | uspto-grants-1986_03 |
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