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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167672Generated: November 1, 2026

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

https://huagongshe.com/reaction/1167672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
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

10 g (42 mmol) of (2S)-3-amino-2-benzyloxycarbonylaminopropionic acid are shaken in an autoclave for 3 days, at an N2 pressure of 20 atm., in a mixture consisting of 100 ml of dioxane, 100 ml of isobutylene and 8 ml of conc. H2SO4. Excess isobutylene is blown off and 150 ml of diethyl ether and 150 ml of a saturated solution of NaHCO3 are added to the remaining solution. The phases are separated and the aqueous phase is extracted twice with 100 ml of diethyl ether on each occasion. The combined organic phases are washed with 2×100 ml of H2O and dried over Na2SO4. 9.58 g (78%) of (1.6) are obtained as a pale yellow oil after the solvent has been removed in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620820B2
Source datasetuspto-grants-2003_09
ORD IDord-3146acb983ed42bcb1df3da1f9dbd02d
Source noteuspto-grants-2003_09