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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007492Generated: October 28, 2026

Triphenylphosphine dibromide → 4-(3-Cyclohexylmethyl-1H-indol-5-yloxy)-3,5-bis-trifluoromethyl-benzyl bromide

https://huagongshe.com/reaction/1007492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphine dibromideHCID 70579—
Reactant4-(3-Cyclohexylmethyl-1H-indol-5-yloxy)-3,5-bis-trifluoromethyl-benzyl alcoholHCID 59060961—
SolventAcetonitrileHCID 6342—
Product4-(3-Cyclohexylmethyl-1H-indol-5-yloxy)-3,5-bis-trifluoromethyl-benzyl bromideHCID 22669879—

Reaction Steps

Preparation is carried out in analogy to the procedure of Example VII from 2.0 g (4.18 mmol) of benzyl alcohol derivative from Example XXI and 2.82 g (6.69 mmol) of dibromotriphenylphosphorane in 40 ml of acetonitrile. After stirring for 3 hours at room temperature, 0.3 equivalent of dibromotriphenylphosphorane is again added. The mixture is additionally stirred for 5 hours at 70° C. and afterwards overnight at room temperature. The purification of the product is carried out on silica gel using toluene as eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794406B2
Source datasetuspto-grants-2004_09
ORD IDord-cb7d2592398a405e958dd933132cd94a
Source noteuspto-grants-2004_09