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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855227Generated: October 28, 2026

Hydrochloric Acid → HCID 69341999, compound

https://huagongshe.com/reaction/855227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-tert-ButylbenzaldehydeHCID 70324—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 16219122HCID 16219122—
SolventMethanolHCID 887—
ProductHCID 69341999HCID 6934199979.5%

Reaction Steps

618 mg of [rac]-2-(4-chloro-phenyl)-propylamine hydrochloride (3 mmol) were dissolved in 8 ml methanol at rt and treated with 415 mg of potassium carbonate (3 mmol) and after 5 min stirring treated with 0.755 ml of 4-tert-butylbenzaldehyde (4.5 mmol). After 30 min stirring at rt, the reaction mixture was refluxed for 3 h, and After cooling down to rt, treated with 170 mg (4.5 mmol) sodium borohydride in portions. After 10 min at rt, the reaction mixture was refluxed for 20 h. After cooling down to rt, the reaction mixture was treated with 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 753 mg light brown oil (79%). MS(ISP) 316.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-765fd01428b24eaf97e2330be03aa38d
Source noteuspto-grants-2007_08