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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009281Generated: October 31, 2026

Water → (2S)-2-[(R)-[(4-bromophenyl)-(4-fluorophenyl)-methyl]-amino}-4-methylpentan-1-ol

https://huagongshe.com/reaction/1009281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,4-DibromobenzeneHCID 7804—
Reactant2-[(4-Fluorobenzylidene)-amino]-4-methylpentan-1-olHCID 67298395—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product(2S)-2-[(R)-[(4-bromophenyl)-(4-fluorophenyl)-methyl]-amino}-4-methylpentan-1-olHCID 67298593—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1,4-dibromobenzene (11.4 g, 48.35 mmol) in ether (120 mL) at −30° C. was added n-butyllithium (24.2 mL, 2.0M cyclohexane solution) over 10 minutes. The reaction mixture was stirred for 45 minutes, whereupon a solution of (S) 2-[(4-fluorobenzylidene)-amino]-4-methylpentan-1-ol (maximum 2.16 g, 9.67 mmol from the previous step) in ether (30 mL) was added dropwise. After 2 hours, during which the reaction mixture was allowed to warm to 0° C., water (200 mL) was added. The product was extracted with ethyl acetate (150 mL), washed with brine (100 mL), dried over MgSO4, filtered, concentrated in vacuo, and purified on a short plug of silica gel (20% ethyl acetate/hexane elution) to give (2S)-2-{(R)-[(4-bromophenyl)-(4-fluorophenyl)-methyl]-amino}-4-methylpentan-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973037B2
Source datasetuspto-grants-2011_07
ORD IDord-1d3195408afd430cb0d6c59c0d9f5003
Source noteuspto-grants-2011_07