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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973311Generated: October 29, 2026

Trifluoroacetic acid → HCID 20314460, compound

https://huagongshe.com/reaction/973311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantThiopheneHCID 8030—
ReactantHCID 20314474HCID 20314474—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 20314460HCID 20314460—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A mixture of thiophene (8.7 g.) and acetic anhydride (60 ml.) is added to a stirred suspension of 4-(4-chlorophenyl)-(diacetoxyiodo)benzene (21.7 g.) in a mixture of acetic anhydride (50 ml.) and trifluoroacetic acid (15 ml.) below -10° C. during 1 hour. The mixture is stirred at -10° C. for 2 hours, at ambient temperature for 18 hours and is then filtered. The filtrate is concentrated to small volume in vacuo, and ether is added. The solid so formed is filtered off and crystallised from toluene to give 4-(4-chlorophenyl)-phenyl-2-thienyliodonium trifluoroacetate (13.7 g.), m.p. 175°-177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04055595
Source datasetuspto-grants-1977_10
ORD IDord-07508b027d284a738035660ac5d141f6
Source noteuspto-grants-1977_10