HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284643Generated: October 29, 2026
Propargyl bromide → 5-benzhydrylthio-2-(2-propynyl)-2H-tetrazole
https://huagongshe.com/reaction/1284643
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178420440 | HCID 178420440 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-benzhydrylthio-2-(2-propynyl)-2H-tetrazole | HCID 13051170 | 42.9% |
Reaction Steps
To a solution of 5-benzhydrylthio-1H-tetrazole (29 g) in tetrahydrofuran (145 ml) were added triethylamine (12.0 g) and 2-propynyl bromide (19.3 g) at room temperature. The resulting mixture was stirred for 2.5 hours at 40° to 45° C. The reaction mixture was filtered and the filtrate was evaporated. The residue was shaken with a mixture of ethyl acetate and water. The ethyl acetate layer was separated, washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and then evaporated. The residual oil (27.7 g) was subjected to column chromatography on silica gel, and eluted with a mixture of n-hexane, chloroform and ethyl acetate (5.5:4.5:0.5), to give 5-benzhydrylthio-2-(2-propynyl)-2H-tetrazole (14.2 g), mp 85° to 86° C.
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-ff45d962bded428baf6716c7c033e03f |
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| Source note | uspto-grants-1986_01 |
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