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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633796Generated: October 30, 2026

Ethyl Acetate → (6-methoxy-3,4-dihydro-2H-1-oxa-5,9-diaza-phenanthren-3-yl)-methanol

https://huagongshe.com/reaction/633796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLithium ChlorideHCID 433294—
ReactantSodium borohydrideHCID 4311764—
Reactant6-methoxy-2H-1-oxa-5,9-diaza-phenanthrene-3-carboxylic acid methyl esterHCID 71118738—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(6-methoxy-3,4-dihydro-2H-1-oxa-5,9-diaza-phenanthren-3-yl)-methanolHCID 7111794574%

Reaction Steps

Sodium borohydride (417 mg, 11.03 mmol, 5.0 eq) is added at 0° C. to a stirred suspension of 6-methoxy-2H-1-oxa-5,9-diaza-phenanthrene-3-carboxylic acid methyl ester (600 mg, 2.20 mmol, 1.0 eq) in methanol (60 mL), followed by lithium chloride (467 mg, 11.03 mmol, 5.0 eq). After 3 hours stirring at room temperature, solvent is removed and the residue is dissolved in methanol (60 mL) and treated with 10% palladium on activated carbon (100 mg, 0.09 mmol, 0.05 eq). The resulting mixture is stirred under hydrogen flow (3 bars) at room temperature for 3 hours. The catalyst is then removed by filtration and the solution is concentrated to give a residue that is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate, 4:1 to 3:1, v/v) to afford (6-methoxy-3,4-dihydro-2H-1-oxa-5,9-diaza-phenanthren-3-yl)-methanol as a white solid (400 mg, 74% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321788B2
Source datasetuspto-grants-2016_04
ORD IDord-98d59702339a41b892c686e9311591c4
Source noteuspto-grants-2016_04