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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784442Generated: October 30, 2026

Carbon tetrabromide → HCID 86610733, compound

https://huagongshe.com/reaction/1784442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 86610732HCID 86610732—
SolventDichloromethaneHCID 6344—
ProductHCID 86610733HCID 8661073398%

Reaction Steps

To a solution of 6-methoxy-1-(R)-(2-hydroxyethyl)-3,4-dihydro-1H-isoquinoline-trifluoroacetamide (330 mg, 1.09 mmol) obtained in step (b) of Example 190 and carbon tetrabromide (542 mg, 1.63 mmol) in dichloromethane (5 ml) was added gradually triphenyl phosphine (343 mg, 1.31 mmol) with stirring under cooling in a water bath. The resulting mixture was further stirred at room temperature, and after confirming the disappearance of the starting material by thin layer chromatography, the reaction mixture was evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of hexane and ethyl acetate (80:20) as the eluent to afford the title compound (390 mg, yield: 98%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504393B2
Source datasetuspto-grants-2009_03
ORD IDord-04725603260849d48bb508a803e3335e
Source noteuspto-grants-2009_03