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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572727Generated: November 1, 2026

Sodium borohydride → methyl 8-(1-hydroxyethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate

https://huagongshe.com/reaction/572727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantmethyl 8-acetyl-2-morpholino-4-oxo-4H-chromene-6-carboxylateHCID 58235004—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Productmethyl 8-(1-hydroxyethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxylateHCID 5823501376.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Sodium tetrahydroborate (82 mg, 2.16 mmol) was added to a solution of methyl 8-acetyl-2-morpholino-4-oxo-4H-chromene-6-carboxylate (650 mg, 1.96 mmol) in methanol (20 mL) and DCM (10 mL) at −10° C. After 15 min of stirring at −10° C., the reaction mixture was quenched with water (25 mL). The volatiles were removed and the aqueous layer extracted twice with DCM. The combined organics phases were washed with brine, dried over magnesium sulfate and concentrated. The residue was triturated with diethylether and the solid collected by filtration to give methyl 8-(1-hydroxyethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate (500 mg, 76%) as a brown solid, which used for the next step without further purification. Mass Spectrum: M+H+ 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029374B2
Source datasetuspto-grants-2015_05
ORD IDord-f9e659ad27bb4dc69a40fc92174fcbd1
Source noteuspto-grants-2015_05