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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879811Generated: October 25, 2026

Glycine tert-butyl ester → Tert-butyl 2-{[1,3-bis(acetyloxy)propan-2-yl]amino}acetate

https://huagongshe.com/reaction/1879811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycine tert-butyl esterHCID 151417—
Reactant1,3-DiacetoxyacetoneHCID 243418—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ProductTert-butyl 2-{[1,3-bis(acetyloxy)propan-2-yl]amino}acetateHCID 8663576238.7%

Reaction Steps

To a solution of 3-(acetyloxy)-2-oxopropyl acetate (3.0 g, 17.24 mmol) on dichloroethane (70 ml) was added tert-butyl 2-aminoacetate (2.35 ml, 17.24 mmol). The reaction was stirred for 90 minutes before sodium triacetoxyborohydride (5.5 g, 25.86 mmol) was added and stirring was continued for 18 hours. The reaction was quenched by the addition of saturated sodium hydrogen carbonate solution and the crude product was extracted into dichloromethane. The organic phase was separated, dried over MgSO4, filtered and concentrated in vacuo. The title compound was purified by silica column chromatography eluting with 0-40% EtOAc:Hept to yield the title compound (1.93 g, 38% yield). 1H NMR (250 MHz, CHLOROFORM-d) δ 3.96-4.26 (4H, m), 3.30-3.45 (2H, m), 3.06 (1H, quin, 5.4 Hz), 2.09 (6H, s), 1.47 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318705B2
Source datasetuspto-grants-2012_11
ORD IDord-02652555ff614547b7eb353120993a0c
Source noteuspto-grants-2012_11