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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734342Generated: October 29, 2026

Acetonitrile → HCID 11436331, compound

https://huagongshe.com/reaction/734342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactantp-BromoacetophenoneHCID 7466—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantIodo benzene diacetateHCID 12217721—
ProductHCID 11436331HCID 11436331—

Reaction Steps

Trifluoromethanesulfonic acid (6.6 ml) was added to a flask containing iodobenzene diacetate (12.2 g) and MeCN (200 ml) at rt. After 25 min. a solution of 4′-bromoacetophenone (5 g) in MeCN (50 ml) was added and the resultant mixture heated at reflux for 6 h. The reaction was allowed to cool to rt before the solvent was evaporated and the residue partitioned between saturated aqueous Na2CO3 (150 ml) and EtOAc (150 ml). The organic phase was washed with saturated brine (150 ml), dried (MgSO4) and evaporated to give an orange solid. The crude product was purified by column chromatography (silica gel, 50% EtOAc in hexane) to give the title compound (D38) as a pale yellow solid (3.5 g). LCMS electrospray (+ve) 239 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592347B2
Source datasetuspto-grants-2009_09
ORD IDord-6f93e34ccb724e14afcc8710f2f12a7d
Source noteuspto-grants-2009_09