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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620953Generated: November 2, 2026

1,4-Dibromobenzene → HCID 57446955, compound

https://huagongshe.com/reaction/1620953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
ReactantCyclohexaneHCID 8078—
ReactantHCID 57515780HCID 57515780—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 57446955HCID 57446955—

Reaction Steps

Butyllithium (41 mL of a 2.0M cyclohexane solution) was added at −30° C. to a solution of 1,4-dibromobenzene (19.3 g, 81.89 mmol) in ether (250 mL) over 10 minutes. After 1 hour, a solution of (4S)-4-propyl-2-trifluoromethyloxazolidine (3.00 g, 16.38 mmol) was added in ether (50 mL) over 30 minutes via an addition funnel. After 90 minutes of stirring, water (100 mL) was added. The organic phase was washed with brine (100 mL), dried over MgSO4, filtered, and evaporated to dryness. The residue was purified on a plug of silica gel (10-30% ethyl acetate/hexane elution). An approximately 2:1 mixture of diastomers of (2S)-2-[1-(4-bromophenyl)-2,2,2-trifluoroethylamino]-pentan-1-ol at the CF3 residue was observed based on the norvaline methyl triplet at 0.98 ppm (1H NMR).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772336B2
Source datasetuspto-grants-2014_07
ORD IDord-d7edd8ad361d4ed59cc78a7682561699
Source noteuspto-grants-2014_07