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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106844Generated: October 30, 2026

Trifluoroacetic acid → 2-(2-Aminoethyl)-4-bromophenyl benzyl ether

https://huagongshe.com/reaction/1106844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Bromo-2-cyanomethylphenyl benzyl etherHCID 22675467—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Aminoethyl)-4-bromophenyl benzyl etherHCID 17938263108.6%

Reaction Steps

To a mixture of NaBH4 (6.0 g) in THF (100 ml) was added dropwise trifluoroacetic acid (18 ml) at 0° C. (ice bath). 4-Bromo-2-cyanomethylphenyl benzyl ether (10 g) was added and the mixture stirred at ambient temperature for 18 hours. The reaction was quenched with water (100 ml), the pH adjusted to 13 with 2N aqueous NaOH solution, and extracted with diethyl ether. The diethyl ether extracts were dried (MgSO4) and evaporated to give 2-(2-aminoethyl)-4-bromophenyl benzyl ether (11.0 g) as a yellow gum,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057345
Source datasetuspto-grants-2000_05
ORD IDord-a6ebd848c30847d0ae91d9c799703076
Source noteuspto-grants-2000_05