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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191729Generated: October 25, 2026

Acetic Acid → 4-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-ol

https://huagongshe.com/reaction/1191729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(alphaS)-4-Bromo-alpha-methylbenzenemethanamineHCID 852999—
Reactant3-Hydroxy-4-methoxy-3-phenyl-butyraldehydeHCID 59635677—
SolventTetrahydrofuranHCID 8028—
Product4-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-olHCID 59635799—

Reaction Steps

(S)-1-(4-Bromo-phenyl)-ethylamine (0.93 g), NaB(OAc)3 (0.98 g), and acetic acid (0.27 mL) were added in the given order to a solution of 3-hydroxy-4-methoxy-3-phenyl-butyraldehyde (0.90 g) in tetrahydrofuran (20 mL) at ca. 10-15° C. The cooling bath was removed and the mixture was stirred at room temperature for 2 h. Then, water (50 mL) and 1 M aqueous NaOH solution (20 mL) were added and the resulting mixture was stirred for another 30 min. The mixture was extracted with ethyl acetate and the combined extracts were washed with water and brine. After drying (MgSO4), the solvent was removed to give the title compound which was submitted to the subsequent reaction step without further purification. Yield: 1.80 g (quantitative). Mass spectrum (ESI+): m/z=378/380 (Br) [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680093B2
Source datasetuspto-grants-2014_03
ORD IDord-05ad39ab7f664b7387fadaf756537843
Source noteuspto-grants-2014_03