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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963048Generated: October 31, 2026

Hydrogen Bromide → HCID 80147526, compound

https://huagongshe.com/reaction/1963048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantHexaneHCID 8058—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant2-Chloro-6-fluorobenzeneacetyl chlorideHCID 21795735—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductHCID 80147526HCID 8014752676.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 2 M solution of trimethylsilyl-diazomethane in hexane (6.54 ml, 13.07 mmol) cooled to 0° C. under argon was added dropwise a solution of 2-chloro-6-fluoro-phenylacetyl chloride (1.23 g, 5.94 mmol) in 24 ml of a mixture of THF and ACN (1:1). The mixture was stirred at 0° C. for 5 h. Then 48% aqueous hydrobromic acid (5.91 ml, 52.28 mmol) was added dropwise and the solution was stirred at room temperature overnight. Then 40 ml of water were added. The aqueous phase was extracted twice with EA, and the combined organic phases were washed with water, a saturated solution of sodium hydrogencarbonate and brine, dried over sodium sulfate, filtered and evaporated to dryness under reduced pressure. The residue was purified by chromatography on silica gel (cyclohexane/EA, 100:0, then 95:5) to give 1.20 g of the title compound as a white powder having a melting point of 47° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415336B2
Source datasetuspto-grants-2013_04
ORD IDord-1577596bd8a94949ba14809710d59ec3
Source noteuspto-grants-2013_04