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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855182Generated: October 28, 2026

4-tert-Butylbenzaldehyde → HCID 43400715, compound

https://huagongshe.com/reaction/855182

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzaldehydeHCID 70324—
Reactant2-(3-Fluorophenyl)ethanamineHCID 533928—
ReactantSodium borohydrideHCID 4311764—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductHCID 43400715HCID 43400715111.7%

Reaction Steps

0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.20 ml 2-(3-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 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 2:1) to give 478 mg colorless viscous oil (100%). MS (ISP) 286.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-45d128dc23a746e08deb16e3447ba653
Source noteuspto-grants-2007_08