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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086656Generated: October 25, 2026

Trifluoroacetic acid → 3-Formyl-2,4,6-trimethylbenzenesulfonyl fluoride

https://huagongshe.com/reaction/1086656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMesityleneHCID 7947—
ReactantFluorosulfuric acidHCID 24603—
ReactantHCID 178418416HCID 178418416—
SolventAntimony pentafluorideHCID 24557—
Product3-Formyl-2,4,6-trimethylbenzenesulfonyl fluorideHCID 1177600630%

Reaction Steps

18.9 ml of 1,3,5-trimethylbenzene was reacted with 20 ml of fluorosulfonic acid and carbon monoxide in the presence of 10 ml of antimony pentafluoride and 10 ml of trifluoroacetic acid as a solvent at 20° C. for 48 hours in substantially the same manner as that of Example 1. The molar ratio of 1,3,5-trimethylbenzene : fluorosulfonic acid : antimony pentafluoride was 1 : 3.5 : 1.4, while the consumption of carbon monoxide was 2.24 λ. The same analyses as those of Example 1 were made to confirm the formation of 6.9 g of 3-formyl-2,4,6-trimethylbenzenesulfonyl fluoride (compound No. 7) in a yield of 30 % based on 1,3,5-trimethylbenzene. mass spectrum: M+ (m/e)=230.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05030752
Source datasetuspto-grants-1991_07
ORD IDord-d3735b04fd1241c5b40e775bd602b0f6
Source noteuspto-grants-1991_07