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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855213Generated: October 28, 2026

Hydrochloric Acid → HCID 69342220, compound

https://huagongshe.com/reaction/855213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-tert-ButylbenzaldehydeHCID 70324—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69343102HCID 69343102—
SolventMethanolHCID 887—
ProductHCID 69342220HCID 69342220100%

Reaction Steps

4 ml of 4-tert-butylbenzaldehyde (24 mmol), 3.9 g of 2-(2-fluoro-5-trifluoromethyl -phenyl)-ethylamine hydrochloride (16 mmol) and 2.2 g of potassium carbonate (18.1 mmol) were suspended in 55 ml methanol at rt, and after stirring for 30 min at rt, were refluxed for 2.5 h. After cooling down to rt, 0.91 (24 mmol) of sodium borohydride were added and after stirring for 5 min at rt, the reaction mixture was refluxed for 2.5 h. After cooling down to rt, the reaction mixture was treated with 5 ml 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 (90 g silica gel; EtOAc/heptane 1:4) to give 6.28 g light yellow oil (100%). MS (ISP) 354.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-d34162c7bef54affb5c8c7a551de6395
Source noteuspto-grants-2007_08