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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230212Generated: November 1, 2026

Sulfuric Acid → (S)-tert-Butyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoate

https://huagongshe.com/reaction/2230212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantIsobutyleneHCID 8255—
ReactantSodium BicarbonateHCID 516892—
ReactantZ-Dap-OHHCID 2756313—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product(S)-tert-Butyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoateHCID 1080373178%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423712B1
Source datasetuspto-grants-2002_07
ORD IDord-52185b469ee84f9b94f4639d26d390fe
Source noteuspto-grants-2002_07