HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-(4-tert-butylphenyl)prop-2-enoate → Ethyl 3-(4-(tert-butyl)phenyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-(4-tert-butylphenyl)prop-2-enoate | HCID 53424249 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 3-(4-(tert-butyl)phenyl)propanoate | HCID 10728414 | 93% |
Reaction Steps
The compound 34-2 (64 mg) according to the same procedure as described in Step 1 was dissolved in methanol (10 ml) and to the solution was added a catalytic amount of 10% palladium/carbon, followed by stirring at room temperature under hydrogen gas atmosphere for 2 hours. The resulting mixture was diluted with ether, filtered through celite, and then concentrated under reduced pressure to yield the compound 34-3 (60 mg, 93%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071650B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-0583a8af4848448ca6b46493ffa3f5c9 |
| Source note | uspto-grants-2011_12 |