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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864786Generated: October 30, 2026

4-Fluorobenzaldehyde → HCID 57973859, compound

https://huagongshe.com/reaction/1864786

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68749600HCID 68749600—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 57973859HCID 5797385970.4%

Reaction Steps

Sodium triacetoxyborohydride (470 mg, 2.23 mmol) and then enough acetic acid to bring the pH to 5 were added to a solution of [2-fluoro-5-(1H-indol-5-yl)-benzyl]-(1-methyl-piperidin-4-yl)-amine (250 mg, 0.74 mmol) and 4-fluorobenzaldehyde (183 mg, 1.48 mmol) in 15 mL of 1,2-dichloroethane. The mixture was stirred at ambient temperature overnight, and then it was diluted with dichloromethane, and neutralized with the careful addition of saturated sodium bicarbonate solution. The organic phase was separated and dried over magnesium sulfate, filtered and concentrated to leave the crude product. Chromatography (elution with methanol/ethyl acetate) provided 232 mg of product. LC/MS (long run): Retention time, 6.12 min; (M+H)=446.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625889B2
Source datasetuspto-grants-2009_12
ORD IDord-dd1ce86ac3a94464af934482d2427e88
Source noteuspto-grants-2009_12