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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114825Generated: November 2, 2026

Acetic Acid → HCID 58857938, compound

https://huagongshe.com/reaction/2114825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
ReactantGlycine methyl esterHCID 69221—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 58857940HCID 58857940—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58857938HCID 58857938—

Reaction Steps

A mixture of glycine methyl ester (2.78 g, 22.14 mmol) in anhydrous THF (13.5 mL) was treated sequentially with triethylamine (3.03 mL, 21.55 mmol), a solution of tert-butyl 4-fluorobenzyl{4-[methoxy(methyl)amino]-2-oxobutyl}carbamate (1.50 g, 4.23 mmol) in anhydrous THF (8.5 mL), sodium triacetoxyborohydride (5.11 g, 24.11 mmol), and acetic acid (485 μL, 8.46 mmol). The mixture was stirred at ambient temperature under inert atmosphere for 42 h. Saturated aqueous NaHCO3 solution was added to the reaction which was stirred until gas evolution ceased. The mixture was extracted into EtOAc, and the aqueous layer was saturated with NaCl and extracted into EtOAc again. The combined organic layers were washed with brine, dried over Na2SO4, and concentrated in vacuo to a pale yellow oil. Purification by silica gel chromatography using gradient elution (hexanes to 40% EtOAc/hexanes to EtOAc) afforded the amine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435735B2
Source datasetuspto-grants-2008_10
ORD IDord-bde8a1bdfabb43e68f2bf60078469579
Source noteuspto-grants-2008_10