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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223562Generated: October 31, 2026

1,4-Dibromobenzene → HCID 57446955, compound

https://huagongshe.com/reaction/2223562

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 acetateihexane 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 numberUS07375134B2
Source datasetuspto-grants-2008_05
ORD IDord-b6281c1147ce4af1bc802a08ec285da5
Source noteuspto-grants-2008_05