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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855190Generated: October 29, 2026

4-tert-Butylbenzaldehyde → HCID 68696866, compound

https://huagongshe.com/reaction/855190

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzaldehydeHCID 70324—
Reactant2-(2-Chlorophenyl)ethylamineHCID 83117—
ReactantSodium borohydrideHCID 4311764—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductHCID 68696866HCID 6869686697%

Reaction Steps

0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.215 ml 2-(2-chloro-phenyl)-ethylamine (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 465 mg light yellow oil (97%). MS (ISP) 302.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-785b7d9f1abc42beb5c1cf4b93b46207
Source noteuspto-grants-2007_08