HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236023Generated: October 26, 2026
t-Butyloxycarbonylaspartic acid alpha-benzyl ester → 3-((tert-Butoxycarbonyl)amino)-4-methoxy-4-oxobutanoic acid
https://huagongshe.com/reaction/2236023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | t-Butyloxycarbonylaspartic acid alpha-benzyl ester | HCID 82036 | — |
| Reactant | Trimethylsilyldiazomethane hexane | HCID 86587183 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-((tert-Butoxycarbonyl)amino)-4-methoxy-4-oxobutanoic acid | HCID 14258702 | — |
Reaction Steps
2.0 g (6.18 mmol) of 4-(benzyloxy)-2-[(t-butoxycarbonyl)amino]-4-oxobutanoic acid was dissolved in a solvent mixture of 6 ml of methanol and 12 ml of toluene. 3.7 ml of 2 M trimethylsilyldiazomethane/hexane solution was added to the obtained solution and they were stirred for 3 hours. Additional 0.5 ml of 2 M trimethylsilyldiazomethane/hexane solution was added to the reaction mixture and they were stirred for 1 hour. The solvent was evaporated under reduced pressure. The residue was dissolved in 20 ml of ethanol. 2.0 g of palladium carbon (10% w/v) was added to the obtained solution, and they were stirred in hydrogen gas atmosphere for 19 hours. After the filtration, the solvent was evaporated under reduced pressure to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07713957B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-820fcd280f6b478fbca844470f90d760 |
|---|
| Source note | uspto-grants-2010_05 |
|---|