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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186180Generated: November 2, 2026

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

https://huagongshe.com/reaction/1186180

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, 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 (intermediate C7A) was obtained as a colourless oil (7.29 g, 98% of theory). MS (ISP): m/z=368.1, 370.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673894B2
Source datasetuspto-grants-2014_03
ORD IDord-b968fff512704f60b3a87226f70e76c5
Source noteuspto-grants-2014_03