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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284633Generated: October 30, 2026

Hydrochloric Acid → 2-[5-(Benzylsulfanyl)-1H-tetrazol-1-yl]ethan-1-ol

https://huagongshe.com/reaction/1284633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2-Hydroxyethyl)hydrazinecarbothioamideHCID 20252217—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 54026318HCID 54026318—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[5-(Benzylsulfanyl)-1H-tetrazol-1-yl]ethan-1-olHCID 20252209—

Reaction Steps

A mixture of 4-(2-hydroxyethyl)thiosemicarbazide (10.3 g), benzyl chloride (10.6 g), water (30 ml) and methanol (60 ml) was stirred for 20 hours at room temperature to give a homogeneous solution containing benzyl N-(2-hydroxyethyl)thiocarbazimidate. The solution was ice-cooled and thereto was little by little added sodium nitrite (5.24 g) with stirring and then dropwise added conc. hydrochloric acid (3.5 ml) over a period of 30 mimetes. The resulting mixture was stirred for an hour under ice-cooling. To the reaction mixture were added potassium carbonate (18 g) and water (30 ml). The mixture was stirred and then concentrated under reduced pressure. The concentrate was extracted with chloroform and the extract was washed with water, dried over magnesium sulfate and then evaporated under reduced pressure. The residual oil was subjected to column chromatography on silica gel. The fractions containing the object compound were collected to give an oil of 1-(2-hydroxyethyl)-5-benzylthio-1H-tetrazole (12.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563524
Source datasetuspto-grants-1986_01
ORD IDord-f3bfbe777e8c4ccbb086a8c94e6fb708
Source noteuspto-grants-1986_01