HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180713Generated: October 29, 2026
Triethylamine hydrochloride → HCID 23118009, compound
https://huagongshe.com/reaction/1180713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 10444178 | HCID 10444178 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 23118009 | HCID 23118009 | 97.8% |
Reaction Steps
Four grams (16.8 mmol) of N-(2-methoxyphenyl)-2,2,2-trifluoroacetimidoyl chloride obtained in Example 9, 1.98 g (30.2 mmol) of sodium azide, 1.16 g (8.42 mmol) of triethylamine hydrochloride, and 40 ml of toluene were introduced into a 100 ml flask and reacted at 80° C. for 14 hours. After the reaction, the reaction solution was cooled to room temperature and washed with water (30 ml×2). The organic phase was dried over anhydrous magnesium sulfate for 1 hour, filtered, and then subjected to solvent removal by evaporation. The crude product thus obtained was purified by column chromatography (silica gel, ethyl acetate:hexane=3:7), resulting in 4.01 g of 1-(2-methoxyphenyl)-5-(trifluoromethyl)-1H-tetrazole as a pale yellow oil (yield: 97.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07282609B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-db05ce80b84940e08a2a9be7f855aec2 |
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| Source note | uspto-grants-2007_10 |
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