HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653823Generated: November 3, 2026
Triethylamine hydrochloride → HCID 178442550, compound
https://huagongshe.com/reaction/1653823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 20080518 | HCID 20080518 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178442550 | HCID 178442550 | 68.2% |
Reaction Steps
3 g of (RS)-7(4,5-diphenyl-2-oxazolyl)-2-methylheptanenitrile in 30 cm3 of dimethylformamide are treated with twice 1.7 g of sodium azide and twice 3.6 g of triethylamine hydrochloride under the (time and temperature) conditions defined in Example 1. After treatment, the product of the reaction is chromatographed on a column 2 cm in diameter containing 78 g of silica gel (50 to 200μ). The column is eluted, collecting 200 cm3 fractions, with 1 liter of diisopropyl ether and then with 1.6 liters of a diisopropyl ether/ethyl acetate (95:5 by volume) mixture. The fractions from the last eluent mixture are concentrated to dryness under reduced pressure (0.2 kPa). 2.3 g (68%) of (RS)-5-[7-(4,5-diphenyl-2-oxazolyl)-2-heptyl]-1H-tetrazole are obtained in the form of a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403852 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-8165d3b2d32b47ff8317466058bab2cd |
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| Source note | uspto-grants-1995_04 |
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