HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[5-(2,4-Diisobutoxybenzoyl)-2-isobutoxyphenyl]acetic acid → 2-[5-(2,4-Diisobutoxybenzyl)-2-isobutoxyphenyl]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[5-(2,4-Diisobutoxybenzoyl)-2-isobutoxyphenyl]acetic acid | HCID 17816564 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[5-(2,4-Diisobutoxybenzyl)-2-isobutoxyphenyl]acetic acid | HCID 17816459 | 72.2% |
Reaction Steps
In 2 ml of ethanol is dissolved 200 mg of 2-[5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenyl]acetic acid. After adding 40 mg of 5% palladium-carbon, the mixture thus obtained is stirred at ambient temperature for one hour in a stream of hydrogen gas. The reaction mixture is filtered with Celite, and the solvent is distilled off under reduced pressure from the filtrate. The residue thus obtained is purified by silica gel column chromatography [eluent; n-hexane:ethyl acetate=4:1] to obtain 140 mg of 2-[5-(2,4-diisobutoxybenzyl)-2-isobutoxyphenyl]acetic acid as a colorless oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07314888B1 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-e810e911102646f3a6e08da4d5ce5858 |
| Source note | uspto-grants-2008_01 |