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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007471Generated: October 28, 2026

Water → HCID 18539369, compound

https://huagongshe.com/reaction/1007471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,5-Dibromo-4-HydroxybenzaldehydeHCID 18100—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
SolventPyridineHCID 1049—
ProductHCID 18539369HCID 18539369—

Reaction Steps

14.73 ml of triflic anhydride is added, under inert gas and at 0° C., to 19.0 g of 3,5-dibromo-4-hydroxy-benzaldehyde in 100 ml of pyridine. Agitation is carried out for 1 hour while allowing the temperature to return to ambient, the reaction medium is poured into water and the aqueous phase is extracted with 3 times 150 ml of dichloromethane. The organic phases are dried and evaporated to dryness under reduced pressure. 23.83 g of crude product is obtained which is purified by filtration chromatography using a cyclohexane/ethyl acetate mixture 1/1 as eluant. In this way 23.83 g of expected product is obtained. Rf: 0.71, cyclohexane/ethyl acetate 1/1. The operation is carried out in an equivalent manner for the preparation of the following triflates of general formula II

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794415B2
Source datasetuspto-grants-2004_09
ORD IDord-a6d8a8dea26441e3937ba6d439751526
Source noteuspto-grants-2004_09