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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215669Generated: October 31, 2026

Sodium borohydride → HCID 516469, compound

https://huagongshe.com/reaction/2215669

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 numberUS07109338B2
Source datasetuspto-grants-2006_09
ORD IDord-ac0b52c48f8c4a9f8f515317d73f1513
Source noteuspto-grants-2006_09