Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855180Generated: October 29, 2026

4-tert-Butylbenzaldehyde → HCID 68564049, compound

https://huagongshe.com/reaction/855180

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzaldehydeHCID 70324—
Reactantp-MethylphenethylamineHCID 76751—
ReactantSodium borohydrideHCID 4311764—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductHCID 68564049HCID 68564049100%

Reaction Steps

0.39 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.22 ml 2-p-tolyl-ethylamine (1.5 mmol) were dissolved in 4.5 ml methanol and after stirring for 30 min at rt, were refluxed for 2.5 h. After cooling down to rt, 85 mg (2.25 mmol) sodium borohydride were added and after stirring for 5 min at rt, the reaction mixture was then refluxed for 2.5 h. After cooling down to rt, the reaction mixture was treated with 4 drops 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel; EtOAc/heptane 1:1) to give 480 mg light yellow viscous oil (100%). MS (ISP) 282.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-29d72a8557b04c368ccd43c84c699d2e
Source noteuspto-grants-2007_08