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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213815Generated: October 26, 2026

HCID 10156578, compound → 3-Amino-6-hydroxy-7-methoxynaphthalene-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2213815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10156578HCID 10156578—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-Amino-6-hydroxy-7-methoxynaphthalene-2-carboxylic acid tert-butyl esterHCID 1206273897.9%

Reaction Steps

A solution of 4.7 g (12.0 mmol) of 3-amino-6-benzyloxy-7-methoxynaphthalene-2-carboxylic acid tert-butyl ester and 2.0 g of 10% Pd/C in 40 mL of DMF and 100 mL of methanol is shaken on Parr shaker at 40 psi for 18 hours. The catalyst is filtered through a pad of Celite, washed with methanol and solvent is evaporated to yield a residue which is dissolved in methylene chloride. This is then filtered through a short pad of Magnesol and washed with methylene chloride and ethyl acetate. The filtrate is evaporated to yield 3.4 g of 3-amino-6-hydroxy-7-methoxy-naphthalene-2-carboxylic acid tert-butyl ester as a yellow solid, mp 262–263° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105531B2
Source datasetuspto-grants-2006_09
ORD IDord-6a07519f79ee4bfe848a19541850bdfc
Source noteuspto-grants-2006_09