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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855184Generated: October 29, 2026

4-tert-Butylbenzaldehyde → HCID 29273664, compound

https://huagongshe.com/reaction/855184

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzaldehydeHCID 70324—
Reactant2-(2-Fluorophenyl)ethylamineHCID 643357—
ReactantSodium borohydrideHCID 4311764—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductHCID 29273664HCID 2927366465%

Reaction Steps

0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.200 ml 2-(2-fluoro-phenyl)-ethyl-amine (1.5 mmol) were dissolved in 4.5 ml methanol at rt, 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 3 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 1:2) to give 280 mg light yellow oil (65%). MS (ISP) 286.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-b07d7ecfa4624493abb18e651dd12c21
Source noteuspto-grants-2007_08