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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476861Generated: October 31, 2026

HCID 19836754, compound → HCID 19836746, compound

https://huagongshe.com/reaction/476861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19836754HCID 19836754—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 19836746HCID 19836746—

Reaction Steps

14 g Ethyl(o-nitro-benzyloxy)acetate were dissolved in 300 ml 96% ethanol and 1.5 g 5% Pd on carbon was added. The mixture was then hydrogenated at normal pressure and room temperature. After completion of the reaction the mixture was filtered and the filtrate was added to 50 ml 4N NaOH and the resulting solution was left at room temperature for 2 hours, whereafter 50 ml 4N HCl were added. The mixture was evaporated, and the residue was stirred with 200 ml acetone. The mixture was filtered. The filtrate was evaporated to give o-amino-benzyloxy acetic acid as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886797
Source datasetuspto-grants-1989_12
ORD IDord-1dc9f22061b74ba9b669b7f12eb9c0b9
Source noteuspto-grants-1989_12