Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671622Generated: October 31, 2026

4-Chlorobenzaldehyde → HCID 25209039, compound

https://huagongshe.com/reaction/1671622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantL-AlaninolHCID 80307—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 25209039HCID 25209039—

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Chloro-benzaldehyde (1.4 g, 0.01 mol) was dissolved in dry ethanol (30 mL) and (S)-(+)-2-amino-1-propanol (0.75 g, 0.01 mol) was added. The reaction mixture was stirred overnight at 60° C. The ethanol was evaporated under reduced pressure to give a colorless oil. The oil was then dissolved in dry methanol (30 mL) and cooled in ice. NaBH4 (0.57 g, 0.015 mol) was added slowly in portions, and the resulting solution was left overnight at room temperature. The solvent was evaporated in vacuo, and the residue was dissolved in water, and extracted with CH2Cl2 (3×20 mL). The organic layers were combined and dried with Na2SO4, filtered and evaporated in vacuo to give colorless oily residue, which was purified by column chromatography (silica gel, CH2Cl2:MeOH, 9:1) to afford colorless oil (III-1, 1.85 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994326B2
Source datasetuspto-grants-2011_08
ORD IDord-505e3e3f79ef4bfd85733365d59bdbef
Source noteuspto-grants-2011_08