HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284645Generated: October 30, 2026
Trifluoroacetic acid → HCID 178456703, compound
https://huagongshe.com/reaction/1284645
Participants
| Role | Name | HCID | Charge |
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| 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 2N 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 | US04563450 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-61bac776d79a49158fecb2c88836b891 |
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| Source note | uspto-grants-1986_01 |
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