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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009294Generated: October 31, 2026

1,4-Dibromobenzene → HCID 57446955, compound

https://huagongshe.com/reaction/1009294

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 numberUS07973037B2
Source datasetuspto-grants-2011_07
ORD IDord-ce1a741ee4664d5d93cbf361d34aaac7
Source noteuspto-grants-2011_07