HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758340Generated: October 29, 2026
p-Anisoyl chloride → HCID 20509822, compound
https://huagongshe.com/reaction/1758340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12803379 | HCID 12803379 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20509822 | HCID 20509822 | 43.8% |
Reaction Steps
1-Methyl-5-(3-aminopropylthio)-1,2,3,4-tetrazole (0.9 g) is dissolved in a mixture of acetone (50 ml) and water (10 ml). To the mixture is added potassium carbonate (0.7 g) and thereto is added dropwise with stirring 4-methoxybenzoylchloride (1.1 g) under ice-cooling. Stirring is continued for 2 hours under ice-cooling. After acetone is distilled off, water is added to the resulting residue and the mixture is extracted with chloroform. The chloroform solution is washed with saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride and dried over sodium sulfate. Chloroform is distilled off and then the residue is purified by column chloratography (Wakogel C-200), followed by eluting with chloroform to give 1-methyl-5-{3-[N-(4-methoxybenzoyl)amino]propylthio}-1,2,3,4-tetrazole (0.7 g), colorless needles (ethyl acetate-ethanol), m.p. 118°-122° C.
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-04edc4d313aa4ec8bce009d229e3fad1 |
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| Source note | uspto-grants-1983_02 |
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