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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218118Generated: October 24, 2026

Benzaldehyde, 3,5-dimethyl- → N-(5-((1R,2S)-2-(3,5-Dimethylbenzylamino)-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamide

https://huagongshe.com/en/reaction/218118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehyde, 3,5-dimethyl-HCID 34225—
ReactantN-(5-((1R,2S)-2-Amino-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamideHCID 58280635—
SolventMethanolHCID 887—
ProductN-(5-((1R,2S)-2-(3,5-Dimethylbenzylamino)-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamideHCID 4462848433%

Reaction Steps

Borane-pyridine complex (160 μL, 1.50 mmol) was added to a methanol solution (5 mL) of an amine (3) (131 mg, 0.50 mmol) and 3,5-dimethylbenzaldehyde (90 μL, 0.65 mmol) at 40° C. and the mixture was stirred for 1.5 hours. The reaction mixture was allowed to cool to room temperature and extracted after addition of water with a mixed solvent (ethyl acetate: methanol=10:1), and the organic layer was washed with saturated aqueous sodium chloride solution. The organic layer was dried and concentrated, and the crude product obtained was purified by amine silica gel column chromatography (eluant:chloroform:methanol=7:1), to give a desired amine (8) as a white solid (62 mg, yield 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198330B2
Source datasetuspto-grants-2012_06
ORD IDord-f6b63811fd6c4cf3b29ec7d1f9687130
Source noteuspto-grants-2012_06