HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006399Generated: October 30, 2026
HCID 12993710, compound → HCID 11737800, compound
https://huagongshe.com/reaction/1006399
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 12993710 | HCID 12993710 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 11737800 | HCID 11737800 | 87.5% |
Reaction Steps
To a solution of methyl 2,4-dichloro-3-(4,5-dihydro-4-methyl-5-oxo-1H-tetrazol-1-yl)benzoate (4.10 g) in dioxane (70 ml), 10N sodium hydroxide (2.0 ml) and water (4ml) were added and the mixture was stirred at 60° C. for 1.5 hours. After concentrating under reduced pressure and the addition of water (50 ml), an aqueous solution of sodium hydroxide was added and washed with ethyl acetate (150 ml). The aqueous layer was acidified with hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with saturated salt water and dried with anhydrous magnesium sulfate. By distilling off of ethyl acetate, the objective 2,4-dichloro-3-(4,5-dihydro-4-methyl-5-oxo-1H-tetrazol-1-yl)benzoic acid (3.42 g, yield 87%) was obtained. mp: 221-225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790810B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-6dd4f671e5b84914b2e04bf4cc2db35c |
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| Source note | uspto-grants-2004_09 |
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