HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852275Generated: October 25, 2026
Triethylamine → (E)-3-(3-methoxyphenyl)acrylic azide
https://huagongshe.com/reaction/1852275
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 3-Methoxycinnamic Acid | HCID 637668 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (E)-3-(3-methoxyphenyl)acrylic azide | HCID 49782297 | 79.1% |
Reaction Steps
To a solution of (E)-3-(3-methoxyphenyl)acrylic acid (20 g, 112 mmol) in benzene (200 ml) was added triethylamine (22.72 g, 224 mmol) followed by DPPA (30.9 g, 112 mmol) at room temperature. The reaction mass was stirred at the same temperature for 18 h. The solvent was evaporated under reduced pressure and the residue was diluted with water and extracted with dichloromethane. Combined organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to get crude compound. The crude compound was purified by conventional column chromatography (Silica gel, 60-120 mesh) using 10% ethyl acetate in pet ether as mobile phase to get the desire compound as white solid (18 g, 79%). 1H NMR (400 MHz, CDCl3): δ ppm 7.73-7.69 (d, J=16 Hz, 1H), 7.33-7.29 (t, J=8 Hz, 1H), 7.26 (s, 1H), 7.14-7.12 (d, J=8 Hz, 1H), 7.05 (s, 1H) 6.98-6.96 (d, J=4 Hz, 1H), 6.43-6.39 (d, J=16 Hz, 1H), 3.86 (s, 3H);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08957203B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-36774318f9f64c51a111e2354364676a |
|---|
| Source note | uspto-grants-2015_02 |
|---|