HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 3-Formyl-2,4,6-trimethylbenzenesulfonyl fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Mesitylene | HCID 7947 | — |
| Reactant | Fluorosulfuric acid | HCID 24603 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Solvent | Antimony pentafluoride | HCID 24557 | — |
| Product | 3-Formyl-2,4,6-trimethylbenzenesulfonyl fluoride | HCID 11776006 | 30% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05030752 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-d3735b04fd1241c5b40e775bd602b0f6 |
| Source note | uspto-grants-1991_07 |