HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758327Generated: November 1, 2026
Cyclohexyl bromide → HCID 13061936, compound
https://huagongshe.com/reaction/1758327
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexyl bromide | HCID 7960 | — |
| Reactant | HCID 20509856 | HCID 20509856 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 13061936 | HCID 13061936 | 55.1% |
Reaction Steps
1-Methyl-5-(3-mercaptopropyl)thio-1,2,3,4-tetrazole (1.9 g) is dissolved in 1 N aqueous sodium hydroxide (30 ml), and thereto is added dropwise a solution of cyclohexyl bromide (2.0 g) in acetone (20 ml) with stirring under ice-cooling. After the addition, the mixture is stirred at room temperature for 3 hours. Acetone is distilled off and water is added to the residue, and the mixture is extracted with ether. The ether solution is washed with diluted aqueous sodium hydroxide and saturated aqueous sodium chloride, and dried over sodium sulfate. After ether is distilled off, the residue is purified by column chromatography (Kieselgel 60), followed by eluting with n-hexane-ether (4:1) to give 1-methyl-5-(3-cyclohexylthiopropyl)thio-1,2,3,4-tetrazole (1.5 g), colorless liquid, nD18 =1.5433.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04372953 |
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| Source dataset | uspto-grants-1983_02 |
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| ORD ID | ord-535fb39431f34229b0af718833c9e057 |
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| Source note | uspto-grants-1983_02 |
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