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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantTriethylamineHCID 8471—
ReactantHCID 178420440HCID 178420440—
SolventTetrahydrofuranHCID 8028—
Product5-benzhydrylthio-2-(2-propynyl)-2H-tetrazoleHCID 1305117042.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563450
Source datasetuspto-grants-1986_01
ORD IDord-ff45d962bded428baf6716c7c033e03f
Source noteuspto-grants-1986_01