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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263452Generated: November 1, 2026

Sodium borohydride → HCID 516469, compound

https://huagongshe.com/reaction/1263452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21952567HCID 21952567—
ProductHCID 516469HCID 516469—

Reaction Steps

To an ethanolic solution of 5-ethyl-8-isopropyl-5,10-dihydro-11H-indeno[1,2-b]quinolin-10,11-dione (500 mg, 1,58 mmol) was added sodium borohydride (62 mg, 1.64 mmol) in portions followed by stirring at room temperature for 1 hour. After removing ethanol, the reaction mixture was diluted with water and extracted with chloroform twice. The combined organic layers were washed with saturated sodium chloride solution and dried with sodium sulfate followed by evaporating to remove chloroform. The title compound was obtained by crystallizing the residue from acetone-diethyl ether mixture. 1H-NMR(CDCl3)δ 1.35(6H,d,CH(CH3)2), 1.72(3H,t,NCH2CH3), 3.11(1H,septet,CH), 4.79(2H,q,NCH2), 5.86(1H,s,H-11), 7.52-7.63(3H,m,Ar-H), 7.85(1H,dd,H-9)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541470B1
Source datasetuspto-grants-2003_04
ORD IDord-5bc0af72d9954a84a754c2fa922a8a9f
Source noteuspto-grants-2003_04