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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709260Generated: October 31, 2026

Carbon tetrabromide → HCID 86744151, compound

https://huagongshe.com/reaction/1709260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 14835745HCID 14835745—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86744151HCID 86744151—

Reaction Steps

11.54 g of triphenylphosphine was added to a solution of 7.83 g of (E)-3-(3-triphenylmethylaminophenyl)allyl alcohol and 14.59 g of carbon tetrabromide dissolved in 60 ml of tetrahydrofuran, with ice-cooling. The mixture was stirred for 1 hour at the same temperature to obtain a tetrahydrofuran solution of (E)-(3-triphenylmethylaminophenyl)allyl bromide. To this solution were added 4.45 g of triethylamine and 6.47 g of 3-nitro-5-(piperazin-1-yl)-10,11-dihydro-5H-dibenzo[a,d]cycloheptene, with ice-cooling. The mixture was stirred for 5 hours at room temperature. To the reaction mixture was added 200 ml of water and the mixture was extracted with chloroform. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by a column chromatography (eluant: n-hexane/acetone=3/1) to obtain 7.8 g of light yellow oily 3-nitro-5-[4-{(E)-3-(3-triphenylmethylaminophenyl)allyl}piperazin-1-yl]-10,11-dihydro-5H-dibenzo[a,d]cycloheptene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04948796
Source datasetuspto-grants-1990_08
ORD IDord-78786cc04ac64214be1b42c51aa51a42
Source noteuspto-grants-1990_08