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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408592Generated: October 30, 2026

4-Chlorobenzaldehyde → HCID 28684408, compound

https://huagongshe.com/reaction/408592

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantN-(2-aminoethyl)acetamideHCID 66082—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 28684408HCID 28684408—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-(2-amino-ethyl)-acetamide (1.2 eq.) in MeOH were added NaHCO3 (1.5 eq.) and 4-chlorobenzaldehyde (1 eq.). The reaction was refluxed for 4 h, then cooled to 0° C. NaBH4 (1.2 eq.) was added portionwise. The reaction was stirred for 1 h at 0° C., then 15 h at 20° C. The crude was concentrated under reduced pressure then partitioned between water and DCM. The aqueous layer was then extracted twice with DCM. The organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc: 1/0 to 0/1) to afford N-[2-(4-chloro-benzylamino)-ethyl]-acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759334B2
Source datasetuspto-grants-2014_06
ORD IDord-d2e705cb6e6349209f47db9c89b5a911
Source noteuspto-grants-2014_06