HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990621Generated: October 29, 2026
Sodium Methoxide → HCID 178527384, compound
https://huagongshe.com/reaction/990621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 12056494 | HCID 12056494 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178527384 | HCID 178527384 | 61.9% |
Reaction Steps
To a solution of 7 g (0.019 mol) 3-(bromodifluoromethylsulfonyl)-1-(N,N-diethylcarbamoyl)-1,2,4-triazole, prepared as in Example 1, in 50 ml methanol at room temperature was added 6.7 ml (0.029 mol) of a 25% w/v solution of sodium methoxide in methanol and the mixture was stirred for 2 h. The reaction mixture was then evaporated and the residue was triturated with ether. The resulting solid was collected by filtration, washed with ether and air-dried. A solution of the above solid in 50 ml water was acidified with concentrated hydrochloric acid and the mixture was extracted with ethyl acetate. The resulting organic layer was washed with saturated sodium chloride solution, dried over MgSO4 and evaporated to give 3.08 g (61% yield) of the desired 3-(bromodifluoromethylsulfonyl)-1,2,4-triazole as a white solid with a melting point of 176-177° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06461997B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-2a3c01b2d8084e45bfdc3dfe07098ee6 |
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| Source note | uspto-grants-2002_10 |
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