HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484814Generated: October 31, 2026
Hydrogen Bromide → HCID 178420440, compound
https://huagongshe.com/reaction/484814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178456704 | HCID 178456704 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178420440 | HCID 178420440 | — |
Reaction Steps
To a mixture of the crude product of 3-benzhydrylisothiosemicarbazide hydrobromide from (1) above, water (2.3 l), conc. hydrochloric acid (126 g) and toluene (900 ml) was dropwise added a solution of sodium nitrite (83.5 g) in water (200 ml) and the resulting mixture was stirred for 1.5 hours at 10° to 15° C. The reaction mixture was extracted with ethyl acetate. The organic layer was added to water (1 l) and adjusted to pH 9.5 with 4N aqueous solution of sodium hydroxide. The separated aqueous layer was then adjusted to pH 2.5 with 10% hydrochloric acid and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried and evaporated to give a residue, which was washed with a mixture of n-hexane and isopropyl ether (2:1) and air-dried to give 5-benzhydrylthio-1H-tetrazole (127.22 g), mp. 132° to 134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04533738 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-056dad8a4d004eeda8bea0746e64fe28 |
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| Source note | uspto-grants-1985_08 |
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