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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325908Generated: October 29, 2026

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

https://huagongshe.com/reaction/325908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium NitrateHCID 24268—
ReactantN-(2-Hydroxyethyl)hydrazinecarbothioamideHCID 20252217—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[5-(Benzylsulfanyl)-1H-tetrazol-1-yl]ethan-1-olHCID 2025220983.1%

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 nitrate (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 numberUS04443443
Source datasetuspto-grants-1984_04
ORD IDord-6ed170a0e7614c8c9339b521958c3881
Source noteuspto-grants-1984_04