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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484728Generated: October 29, 2026

Benzyl Bromide → HCID 23326074, compound

https://huagongshe.com/reaction/484728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 2960505HCID 2960505—
SolventAcetonitrileHCID 6342—
ProductHCID 23326074HCID 2332607499.2%

Reaction Steps

To a stirred mixture of 89.2 parts of α,α-bis(4-fluorophenyl)-4-pyridinemethanol and 720 parts of acetonitrile were added dropwise 56.5 parts of (bromomethyl)benzene at reflux temperature. Upon completion, stirring was continued for 22 hours at reflux. The reaction mixture was allowed to stand over week-end at room temperature. The product was filtered off and set aside. The filtrate was concentrated to a volume of 50 parts. The product was allowed to crystallize. It was filtered off and washed, together with the product which was set aside (see above), with 2,2'-oxybispropane and dried, yielding 139.5 parts (99.2%) of 4-[bis(4-fluorophenyl)hydroxymethyl]-1-(phenylmethyl)pyridinium bromide (intermediate 27).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04533665
Source datasetuspto-grants-1985_08
ORD IDord-a4c08cebed4e4a42aefc62f33611d0da
Source noteuspto-grants-1985_08