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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929499Generated: October 30, 2026

4-Methoxybenzaldehyde → (R)-2-(5-bromo-2-fluoro-phenyl)-2-(4-methoxy-benzylamino)-propan-1-ol

https://huagongshe.com/reaction/1929499

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(R)-2-amino-2-(5-bromo-2-fluorophenyl)propan-1-olHCID 58563010—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
Product(R)-2-(5-bromo-2-fluoro-phenyl)-2-(4-methoxy-benzylamino)-propan-1-olHCID 66931632—

Reaction Steps

A solution of (R)-2-amino-2-(5-bromo-2-fluoro-phenyl)-propan-1-ol (5.0 g, 20.2 mmol) and 4-methoxybenzaldehyde (2.8 g, 20.2 mmol) in 1,2-dichloroethane (150 ml) was treated with sodium triacetoxyborohydride (8.81 g, 40.3 mmol) at room temperature. TLC check (eluent: heptane:ethyl acetate=1:1) showed complete reaction after 30 minutes. For the workup, to the reaction mixture were added ethyl acetate (250 ml) and saturated sodium hydrogen-carbonate solution (100 ml). The aqueous layer was separated, and then extracted with ethyl acetate (250 ml). The combined organic layers were washed with saturated sodium chloride solution (100 ml), thereafter dried over sodium sulfate and evaporated at reduced pressure. After chromatography on Silicycle-Si-amine column using a gradient of heptane and ethyl acetate=100/0 to 50/50 as the eluent, (R)-2-(5-bromo-2-fluoro-phenyl)-2-(4-methoxy-benzylamino)-propan-1-ol was obtained as a colorless oil (7.29 g, 98% of theory). Mass (calculated) C17H19BrFNO2 [368.25]; (found) [M+H]+=368, [M+2-H]+=370.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188079B2
Source datasetuspto-grants-2012_05
ORD IDord-d5e21c5e32244021b2d6c54bb229dda1
Source noteuspto-grants-2012_05