HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905091Generated: October 31, 2026
Triethylamine → 2-Diazonio-3-oxo-1-[(prop-2-en-1-yl)oxy]but-1-en-1-olate
https://huagongshe.com/reaction/1905091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Toluenesulfonyl azide | HCID 13661 | — |
| Reactant | Allyl acetoacetate | HCID 70701 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Diazonio-3-oxo-1-[(prop-2-en-1-yl)oxy]but-1-en-1-olate | HCID 54170651 | 95% |
Reaction Steps
55.4 ml (0.4 mole - 2 equivalents) of triethylamine were added dropwise to a solution, which had been cooled to 0° C., of 28.43 g (0.2 mole) of allyl acetoacetate and 43.39 g (0.22 mole - 1.1 equivalents) of p-toluenesulphonyl azide in 400 ml of anhydrous acetonitrile. The mixture was stirred at 0° C. for 3.5 h, then 50 g of kieselguhr were added, evaporation in vacuo was carried out and then chromatography on 400 g of silica gel (toluene:ethyl acetate 96:4). 31.9 g (95%) of the title compound were obtained as a pale yellow oil, Rf: 0.36 (toluene:ethyl acetate 9:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04841042 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-e35c4e02eeae45339aeec091f483a180 |
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| Source note | uspto-grants-1989_06 |
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