HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259628Generated: October 30, 2026
Thionyl Chloride → HCID 53880412, compound
https://huagongshe.com/reaction/259628
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 53788381 | HCID 53788381 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 53880412 | HCID 53880412 | — |
Reaction Steps
26.2 g (0.1 mol) of 3-allyloxy-4-acetoxy-cinnamic acid are suspended in 90 ml of benzene and 14.6 ml (0.2 mol) of thionyl chloride are added. The reaction mixture is heated to the boil under reflux for 30 minutes. Thereafter the solvent and the excess thionyl chloride are removed by distillation under reduced pressure. The crude 3-allyloxy-4-acetoxycinnamic acid chloride which is left is dissolved in 100 ml of absolute dimethoxyethane, 19.5 g (0.3 mol) of sodium azide are added and the reaction mixture is subsequently stirred for 48 hours at room temperature. The inorganic salts are then filtered off and the filtrate is concentrated under reduced pressure at 30° C. Hereupon, colourless crystals separate out. The crystallisation is completed by addition of ether. 3-Allyloxy-4-acetoxy-cinnamic acid azide of melting point 83°-84° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04038414 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-f0d348cba7114bc99c95c73e06c3f8a5 |
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| Source note | uspto-grants-1977_07 |
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