HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071930Generated: November 2, 2026
Trifluoromethanesulfonic anhydride → HCID 22390454, compound
https://huagongshe.com/reaction/1071930
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | HCID 22390446 | HCID 22390446 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22390454 | HCID 22390454 | — |
Reaction Steps
8.2 ml of triflic anhydride are added at 5° C. to 9.7 g of 2-chloro-4-(4,4-dimethylcyclohexyl)phenol (compound IX.1) in 60 ml of pyridine, the reaction mixture is left to stand for 30 minutes at 0° C., and then the reaction mixture is stirred at room temperature for 12 hours. The reaction mixture is hydrolysed and then extracted with dichloromethane. The organic phase is dried over magnesium sulphate and the solvents are evaporated off under reduced pressure. The residue obtained is taken up in toluene, and then the solvents are evaporated off under reduced pressure. The residue obtained is purified by chromatography on a column of silica gel, eluting with a cyclohexane/ethyl acetate mixture which varies from 100/0 to 99/1 (v/v). 15 g of the compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06908914B1 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-c849e5f47c714cc0bc66f7d97c477071 |
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| Source note | uspto-grants-2005_06 |
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