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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697358Generated: October 31, 2026

Acetonitrile → HCID 66688783, compound

https://huagongshe.com/reaction/1697358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantBis(trifluoroacetoxy)iodobenzeneHCID 102317—
ReactantHCID 66688579HCID 66688579—
SolventWaterHCID 962—
ProductHCID 66688783HCID 66688783—

Reaction Steps

A solution of α,α-diethyl-2-(phenylmethoxy)-benzeneacetamide (Example 266c, 0.77 g) in acetonitrile (6 mL) and water (6 mL) was treated with (bis(trifluoroacetoxy)iodo)benzene (1.113 g) under nitrogen and the reaction stirred at room temperature for 16 h. Further (bis(trifluoroacetoxy)iodo)benzene (1.0 g) was added and the reaction stirred for 3 h. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried (MgSO4), filtered and evaporated. The crude product was purified on SCX resin eluting with methanol (discarded) followed by 7N NH3 in methanol. The basic fractions were collected and the volatiles were removed in vacuo to afford subtitle compound (0.83 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163905B2
Source datasetuspto-grants-2012_04
ORD IDord-ef75cd5a94e84c2fa7311978b521593f
Source noteuspto-grants-2012_04