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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387101Generated: October 30, 2026

HCID 21182946, compound → HCID 21182659, compound

https://huagongshe.com/reaction/1387101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21182946HCID 21182946—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21182659HCID 2118265937.7%

Reaction Steps

3-(4-Cyanobenzyl)-2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophene (50 mg, 0.114 mmol) in THF (2 mL) was treated with lithium aluminum hydride (40 mg) at ambient temperature under argon for 1 h. The reaction was quenched with water (0.5 mL) and a solution of NaOH (1.0 M, 0.5 mL). The stirring was continued for 15 min. The resulting mixture was diluted with brine (30 mL) and extracted with CH2Cl2 (3×30 mL). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. Chromatography with Et3N:MeOH:EtOAc (10:40:50) afforded the product (19 mg, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-3b19c2849f7e461ba67cf8b56abc4a8d
Source noteuspto-grants-2001_07