HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(4-Chlorophenyl)-2-methyl-acryloyl azide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 3-(4-Chlorophenyl)-2-methylprop-2-enoic acid | HCID 235114 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Chlorophenyl)-2-methyl-acryloyl azide | HCID 54276253 | 87.7% |
Reaction Steps
To a solution of 3-(4-chlorophenyl)-2-methyl-acrylic acid (11.2 g, 57 mmol) in 500 mL of acetone at 0° C. is added triethyl amine (9.6 mL, 68 mmol) followed by ethyl chloroformate (6.2 mL, 63 mmol). The solution is allowed to warm to ambient temperatures. After 2 h, sodium azide (5.6 g, 86 mmol) in 35 mL of H2O is added. After addition, the solution is stirred for 2 hours. The solution is diluted with H2O (100 mL). The resulting solid is collected by filtration giving the title compound as a white solid (11.1 g, 50 mmol). 1H NMR (CDCl3, 300 MHz) δ7.67 (s, 1H), 3.38 (m, 4H), 2.10 9s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612075B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-6bcd48efa069475598b0c78c49ceb48f |
| Source note | uspto-grants-2009_11 |