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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253887Generated: November 2, 2026

HCID 68639140, compound → HCID 68628824, compound

https://huagongshe.com/reaction/1253887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68639140HCID 68639140—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 68628824HCID 68628824100.4%

Reaction Steps

To a solution of [tert-butoxycarbonyl-(4-fluoro-2-nitro-benzyl)-amino]-acetic acid (5.11 g, 15.50 mmol) in absolute EtOH (30 mL), was added 10% Pd/C (1.02 g, 20% w/w). The reaction was stirred at r.t. for 5 h under hydrogen atmosphere. After completion of the reaction, as confirmed by TLC, the reaction mixture was filtered through celite bed and was washed with EtOAc (10 mL) and MeOH (10 mL). The solvents were removed in vacuo to afford 2-((2-amino-4-fluorobenzyl) (tert-butoxycarbonyl)amino) acetic acid (4.64 g, 99.9%), which was used as such far the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455479B2
Source datasetuspto-grants-2013_06
ORD IDord-ee6af96a65ac4d51b26bee464739d596
Source noteuspto-grants-2013_06