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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921691Generated: October 30, 2026

Sodium borohydride → HCID 57577369, compound

https://huagongshe.com/reaction/1921691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantDiethyl acetamido(6-octyl-1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)propanedioateHCID 57577370—
SolventEthanolHCID 702—
ProductHCID 57577369HCID 5757736975.6%

Reaction Steps

To a solution of sodium borohydride (75 mg, 2.00 mmol) in 5 ml of ethanol at room temperature is added 2-acetylamino-2-(6-octyl-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-malonic acid diethyl ester (compound 5) (1.00 g, 2.1 mmol) in 5 ml of ethanol. The reaction mixture is stirred at room temperature under argon for an additional hour, quenched by the addition of water (20 mL) and methylene chloride (20 mL). The organic layer is removed and the aqueous layer is extracted with methylene chloride (2×20 mL). The combined organic layers were washed with brine (2×20 mL) and dried over magnesium sulfate and concentrated under vacuum. The residue is purified by column chromatography (silica gel, 20% ethyl acetate in hexanes) to provide 755 mg of compound A (75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173710B2
Source datasetuspto-grants-2012_05
ORD IDord-32b0801000f94920870d7ca21932cfb3
Source noteuspto-grants-2012_05