HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127238Generated: October 26, 2026
1H-1,2,4-Triazole → 4-Chloro-1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one naphthalene-1,5-disulphonate
https://huagongshe.com/reaction/127238
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Naphthalenedisulfonic acid | HCID 3015207 | — |
| Reactant | 1-Bromo-4-chloro-1-(4-chlorophenoxy)-3,3-dimethyl-butan-2-one | HCID 20286562 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Chloro-1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one naphthalene-1,5-disulphonate | HCID 20286577 | 192.6% |
Reaction Steps
268.3 g (0.79 mol) of crude 1-bromo-4-chloro-1-(4-chlorophenoxy)-3,3-dimethyl-butan-2-one were dissolved in 2 l of absolute acetonitrile. 190 g (2.7 mol) of 1,2,4-triazole were added thereto and the mixture was heated for 20 hours under reflux. It was then concentrated by distilling off the solvent in vacuo and the residue was taken up in 1,000 ml of methylene chloride. The mixture was washed three times with 250 ml of water at a time, dried over sodium sulphate and again concentrated in vacuo. The oil which remained was dissolved in 1,000 ml of acetone and a solution of 140 g (0.48 mol) of naphthalenedisulphonic acid in 500 ml of acetone was added. After 30 minutes, the resulting precipitate was filtered off. 285 g (76.6% of theory) of 4-chloro-1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one naphthalene-1,5-disulphonate of melting point 245° C. (with decomposition) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04255434 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-5cb06980892b4e3e94355ccb305ed7cf |
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| Source note | uspto-grants-1981_03 |
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