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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Nitrate | HCID 24268 | — |
| Reactant | N-(2-Hydroxyethyl)hydrazinecarbothioamide | HCID 20252217 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[5-(Benzylsulfanyl)-1H-tetrazol-1-yl]ethan-1-ol | HCID 20252209 | 83.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04443443 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-6ed170a0e7614c8c9339b521958c3881 |
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| Source note | uspto-grants-1984_04 |
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