HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180717Generated: October 30, 2026
Triethylamine hydrochloride → HCID 23131657, compound
https://huagongshe.com/reaction/1180717
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 143681-37-2 | HCID 10332712 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 23131657 | HCID 23131657 | 94.3% |
Reaction Steps
Four grams (15.5 mmol) of N-(naphthalen-1-yl)-2,2,2-trifluoroacetimidoyl chloride obtained in Example 13, 1.84 g (27.9 mmol) of sodium azide, 1.08 g (7.76 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 precipitated for 1 hour in 18 ml of n-hexane while being cooled using an ice bath, followed by filtration and drying, thereby giving 3.86 g of 1-(naphthalen-1-yl)-5-(trifluoromethyl)-1H-tetrazole as a white powder (yield: 94.1%).
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-e1c5ede3723f45bcbe00f0758fa6f99c |
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| Source note | uspto-grants-2007_10 |
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