HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995785Generated: October 30, 2026
Trifluoroacetic acid → HCID 178456703, compound
https://huagongshe.com/reaction/1995785
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | 5-benzhydrylthio-2-(2-propynyl)-2H-tetrazole | HCID 13051170 | — |
| Product | HCID 178456703 | HCID 178456703 | 62.5% |
Reaction Steps
A mixture of 5-benzhydrylthio-2-(2-propynyl)-2H-tetrazole (1.05 g), anisole (1.79 g) and trifluoroacetic acid (9.7 ml) was stirred at 22° C. for 1.5 hours, at 35° C. for an hour, at 50° C. for 1.7 hours and then at room temperature for a further 14 hours. The reaction mixture was filtered and the filtrate was evaporated under reduced pressure. To the residue was added a saturated aqueous solution of sodium bicarbonate (10 ml) and the mixture was adjusted to pH 8.5 with 2 N aqueous solution of sodium hydroxide. The aqueous layer was separated, washed with ethyl acetate (20 ml×2) and thereto was added ethyl acetate. The resulting mixture was adjusted to pH 2.5 with 10% hydrochloric acid. The ethyl acetate layer was separated, washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and then evaporated to give an oil of 2-(2-propynyl)-2H-tetrazole-5-thiol (0.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04405617 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-dddc4b24a9654595816dc509a79479fd |
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| Source note | uspto-grants-1983_09 |
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