HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249578Generated: October 30, 2026
Dimethylformamide → HCID 178477163, compound
https://huagongshe.com/reaction/249578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Chloromethyl thiolacetate | HCID 57186933 | — |
| Reactant | HCID 178527994 | HCID 178527994 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178477163 | HCID 178477163 | — |
Reaction Steps
To a solution of tetrazole-5-thiol (3.00 g : 29.41 mMol.) in dimethylformamide (50 ml) under ice cooling is added sodium hydride (60% suspension in oil : 2.59 q : 64.75 mMol.), and the mixture is stirred under ice cooling for 5 to 6 minutes. To the mixture is added a solution of chloromethyl thiolacetate (4.39 gi 35.26 mMol.) in dimethylformamide (10 ml), and the mixture is stirred at room temperature for 2 hours. The reaction mixture is diluted with 10% hydrochloric acid (11 ml) and water and extracted with ethyl acetate. The extract is washed with brine, dried over sodium sulfate, filtered, and concentrated. The residue is purified by silica gel column chromatography (toluene : ethyl acetate=1:1) and the resulting residue is washed with a mixture of n-hexane and ether to give 5-acetylthiomethylthiotetrazole (2.49 9) as colorless crystals. Yield : 45%, m.p. 90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214037 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-7c1bf5f5d3c2465f9a5cb5db75c2847b |
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| Source note | uspto-grants-1993_05 |
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