HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69557Generated: October 27, 2026
Methoxyacetic Acid → 5-(Methoxymethyl)-1,3,4-thiadiazol-2-amine
https://huagongshe.com/reaction/69557
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methoxyacetic Acid | HCID 12251 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(Methoxymethyl)-1,3,4-thiadiazol-2-amine | HCID 660844 | 81% |
Reaction Steps
To a suspension of thiosemicarbazide a24 (40 g, 0.44 mol, 1 eq) in dioxane (400 ml) at room temperature is added methoxyacetic acid (39.56 g, 0.44 mol, 1 eq) in one portion, and the reaction mixture is heated at 80° C. then phosphorous oxychloride (67.54 g, 0.44 mol, 1 eq) is carefully added over 1.5 hours. After reaction completion (4 hours), water is added and the solution is neutralised to pH=6-7 with sodium hydroxyde pellets. After extraction EtOAc/iPrOH (9/1) and evaporation under vacuum, the residue is recrystallized from MeTHF/iPrOH to afford 51 g of pure 5-(methoxymethyl)-1,3,4-thiadiazol-2-amine a25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822508B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-06c0c059141a44578f5004c4a2aa0a42 |
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| Source note | uspto-grants-2014_09 |
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