HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484813Generated: October 29, 2026
Trifluoroacetic acid → HCID 178456704, compound
https://huagongshe.com/reaction/484813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | 5-benzhydrylthio-1-(2-propynyl)-1H-tetrazole | HCID 13051152 | — |
| Product | HCID 178456704 | HCID 178456704 | 59.3% |
Reaction Steps
A mixture of 5-benzhydrylthio-1-(2-propynyl)-1H-tetrazole (0.35 g), anisole (0.6 g) and trifluoroacetic acid (3.4 ml) was stirred for 30 minutes at 20° C. and then allowed to stand for 45 minutes. The reaction mixture was filtered and the filter cake was washed with isopropyl ether. The filtrate and the washing were combined and evaporated under reduced pressure. After the addition of the residue to a saturated aqueous solution of sodium bicarbonate precooled to 10° C., the resulting mixture was adjusted to pH 8.5 with 2N aqueous solution of sodium hydroxide and washed with ethyl acetate. The washed aqueous layer was adjusted to pH 2.5 with 10% hydrochloric acid under ice-cooling and then extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and evaporated to give 1-(2-propynyl)-1H-tetrazole-5-thiol (95 mg), which is decomposed from 60° to 71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04533738 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-4fa4a12ea36e4a57a1fcaac1b366fc64 |
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| Source note | uspto-grants-1985_08 |
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