HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839271Generated: October 27, 2026
Triethylamine → 2-Diazonio-1-methoxy-3-oxohepta-1,6-dien-1-olate
https://huagongshe.com/reaction/839271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Toluenesulfonyl azide | HCID 13661 | — |
| Reactant | Methyl 3-oxo-6-heptenoate | HCID 366065 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Diazonio-1-methoxy-3-oxohepta-1,6-dien-1-olate | HCID 54075634 | 97% |
Reaction Steps
A solution of p-toluenesulfonyl azide (592 mg; 3 mmol) in 1 ml of acetonitrile was added at room temperature to a solution of 3-oxo-6-heptenoic acid methyl ester (468 mg; 3 mmol) and triethylamine (306 mg; 3 mmol) in 5 ml of acetonitrile. The mixture was stirred for about 2 hours and the solvent was distilled off under a reduced pressure and the product was dissolved in 50 ml of ether. The solution was washed with a 5% aqueous solution of potassium hydroxide until no color remained in the aqueous phase and was further washed with a saturated aqueous solution of sodium chloride. The ether solution was dried over anhydrous magnesium sulfate and was filtered and condensed under a reduced pressure to obtain 530 mg of 2-diazo-3-oxo-6-heptenoic acid methyl ester as a yellow oily product. The crude product can be purified by distillation under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04094886 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-7d2deaeffdb7406c994a28be90ca526a |
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| Source note | uspto-grants-1978_06 |
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