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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339138Generated: October 29, 2026

Methanol → 1-(4-Bromo-2-fluorophenyl)ethan-1-amine

https://huagongshe.com/reaction/339138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-Bromo-2-fluorobenzonitrileHCID 736029—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromo-2-fluorophenyl)ethan-1-amineHCID 1854357644%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 12 g of 4-bromo-2-fluorobenzonitrile (60 mM) in THF (120 ml) were added 75 ml (150 mM) of a 2 M solution of methylmagnesium bromide in diethyl ether at 0° C. The reaction mixture was stirred at 0° C. for 6 h. Then 200 ml of methanol were added gradually to the reaction mixture. Subsequently, 5.7 g (150 mM) of sodium borohydride were added in portions, and the mixture was stirred at room temperature for 16 h. Thereafter, the reaction mixture was concentrated under reduced pressure, and 200 ml of water were added. The pH was adjusted to pH=˜1 with 2 M HCl, and the aqueous solution was extracted with chloroform. Subsequently, the pH was adjusted to pH=˜9 with 2M NaOH, and extraction was effected with chloroform (2×100 ml). The combined chloroform extracts were dried, and the solvent was removed under reduced pressure. 7.3 g (44%) of 1-(4-bromo-2-fluorophenyl)ethanamine were obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889878B2
Source datasetuspto-grants-2014_11
ORD IDord-b6bbb2fab1e442519fd838c44c473ea1
Source noteuspto-grants-2014_11