HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883086Generated: November 1, 2026
Sulfuric Acid → (S)-tert-Butyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoate
https://huagongshe.com/reaction/1883086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Z-Dap-OH | HCID 2756313 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (S)-tert-Butyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoate | HCID 10803731 | 78% |
Reaction Steps
The tert-butyl (S)-3-amino-2-benzyloxycarbonylaminopropionate was prepared as follows. 10 g (42 mmol) of (S)-3-amino-2-benzyloxycarbonylaminopropionic acid were shaken in a mixture of 100 ml of dioxane, 100 ml of isobutylene and 8 ml of conc. H2SO4 in an autoclave under an N2 pressure of 20 atm for 3 days. Excess isobutylene was blown out and 150 ml of diethyl ether and 150 ml of saturated NaHCO3 solution were added to the remaining solution. The phases were separated and the aqueous phase was extracted 2× using 100 ml of diethyl ether each time. The combined organic phases were washed with 2×100 ml of water and dried over Na2SO4 After removal of the solvent in vacuo, 9.58 g (78%) of tert-butyl (S)-3-amino-2-benzyloxycarbonylaminopropionate were obtained as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06759424B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-afb71af9fe644ba3be813ce503a3ed7b |
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| Source note | uspto-grants-2004_07 |
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