HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487809Generated: October 28, 2026
HCID 54294220, compound → HCID 14560589, compound
https://huagongshe.com/reaction/487809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 54294220 | HCID 54294220 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 14560589 | HCID 14560589 | 94% |
Reaction Steps
(S)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-[4-[3-(1,1-dimethylethoxy)-3-oxo-1-propenyl]phenyl]propanoic acid diphenylmethyl ester (1.6 g. 2.8 mmol) and 10% Pd/C (300 mg) in t-butanol (20 mL) was blanketed with hydrogen (1 atm). To prevent the solvent from freezing, a warm water bath (40° C.) was used to heat the reaction mixture. Upon the consumption of 2 equivalents of hydrogen, the mixture was filtered through celite. The celite pad was washed with ethanol (50 mL) and the filtrates combined and concentrated. The residue was purified by recrystallization from hexanes to give (S)-2-[[(1,1-dimethylethoxy) carbonyl]amino]-3-[4-[3-(1,1-dimethylethoxy)3-oxopropyl]phenyl]propanoic acid (1.0 g. 2.6 mmol) in 94% yield, mp. 88.5°-90° C., [α]D +21.2° (0.90% in ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05296608 |
|---|
| Source dataset | uspto-grants-1994_03 |
|---|
| ORD ID | ord-370d4ad4249a4bc5b1770bdc2d39b0c3 |
|---|
| Source note | uspto-grants-1994_03 |
|---|