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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241886Generated: November 1, 2026

Water → HCID 59204831, compound

https://huagongshe.com/reaction/2241886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoron TrichlorideHCID 25135—
ReactantHCID 11662395HCID 11662395—
ReactantAcetone cardiceHCID 18522661—
SolventDichloromethaneHCID 6344—
ProductHCID 59204831HCID 5920483146.3%

Reaction Steps

A stirred solution of 0.38 gram (0.00084 mole) of 2-bromo-3-chloro-5-methoxy-1-{4-[5-(trifluoromethyl)(2-pyridyl)]piperazinyl}benzene and 0.78 gram (0.0021 mole) of n-tetrabutylammonium iodide in 30 mL of methylene chloride was cooled in a dry-ice/acetone bath and 2.1 mL (0.0021 mole, a 1.0M solution in methylene chloride) of boron trichloride was added dropwise. Upon completion of addition the reaction mixture was kept cold in the dry-ice/acetone bath for an additional 30-minute period, then it was allowed to warm to ambient temperature where it stirred during a three-hour period. After this time the reaction mixture was cooled in an ice/water bath and 15 mL of water was added. The organic layer was separated and the aqueous layer was extracted with one 15 mL portion of methylene chloride. The organic layer and the extract were combined and dried with sodium sulfate. The mixture was filtered, and the filtrate was concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel using as eluants: 50% hexane in methylene chloride, then 100% methylene chloride, and finally 2% methanol in methylene chloride. The appropriate fractions were combined and concentrated under reduced pressure, yielding 0.17 gram of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671055B2
Source datasetuspto-grants-2010_03
ORD IDord-ab7f4890cbff4cd990d6504f247c6ee4
Source noteuspto-grants-2010_03