HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid → 3-Carbomethoxy-4-(3-methoxyphenyl)butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid | HCID 589607 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Carbomethoxy-4-(3-methoxyphenyl)butanoic acid | HCID 10658447 | 83.1% |
Reaction Steps
A solution of 21.1 g (84 mmol) of 3-carbomethoxy-4-(3-methoxyphenyl)-3-butenoic acid in 100 ml of acetic acid with 2.11 g of 10% Pd on carbon is shaken under H2 atmosphere until H2 uptake ceases (approximately 4 hours). This is filtered through celite and the filtrate concentrated in vacuo several times from toluene to afford 17.6 g of 3-carbomethoxy-4-(3-methoxyphenyl)butanoic acid in the form of a yellow oil which is used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05468898 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-a131f54ab91a46f0a140d8f163f67720 |
| Source note | uspto-grants-1995_11 |