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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725244Generated: November 2, 2026

Acetic Acid → HCID 28531147, compound

https://huagongshe.com/reaction/1725244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCuminaldehydeHCID 326—
Reactant4-ChlorobenzylamineHCID 66036—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 28531147HCID 28531147105.9%

Reaction Steps

To a solution of 4-chlorobenzylamine (2.83 g, 20.0 mmol) and 4-isopropylbenzaldehyde (2.96 g, 20.0 mmol) in methanol (100 mL) were added acetic acid (4.6 mL, 80 mmol) and sodium cyanoborohydride (1.51 g, 24.0 mmol) and the solution was stirred at room temperature for three days. Water (5 mL) was added and the mixture was concentrated in vacuo. The residue was taken up in ethyl acetate (100 mL) and aqueous 1 M KOH (100 mL) and the phases were separated. The aqueous phase was extracted with ethyl acetate (2×100 mL) and the combined organic phase was washed with brine (100 mL), dried over Na2SO4, and concentrated in vacuo to afford 5.80 g of crude product as a white semicrystalline oil. The product was used in the subsequent reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488844B2
Source datasetuspto-grants-2009_02
ORD IDord-e2cee24aca024f5e91009cbd12cac412
Source noteuspto-grants-2009_02