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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167074Generated: October 30, 2026

Benzaldehyde → HCID 11710661, compound

https://huagongshe.com/reaction/2167074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
Reactant1,4-Bis(3-aminopropyl)piperazineHCID 81629—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductHCID 11710661HCID 11710661—

Reaction Steps

To a solution of 1,4-bis(3-aminopropyl)piperazine (0.513 mL, 2.49 mmol) and benzaldehyde (0.532 mL, 5.24 mmol) in absolute ethanol (20 mL) was added 3 Å molecular sieves (5 g). After stirring the mixture for 12 h at room temperature, sodium borohydride (1.9 g, 49.9 mmol) was added and the mixture was stirred for 12 h at room temperature. Then the reaction mixture was quentched by dropwise addition of water (20 mL) and ethanol was removed under reduced pressure. The aqueous residue was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were extracted with HCl 1N (2×50 mL). The combined aqueous layers were neutralized with NaOH 1N (50 mL) and extracted with CH2Cl2 (3×30 mL). The combined organic layers were dried over MgSO4, evaporated to dryness and the oily residue purified by flash chromatography (neutral aluminium oxide, CH2Cl2/MeOH: 90/10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09044478B2
Source datasetuspto-grants-2015_06
ORD IDord-46ef28cf67254f24b406ef7b1ce9accd
Source noteuspto-grants-2015_06