HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(3-Pyridyl)acryloyl chloride hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-(3-Pyridinyl)-2-propenoic acid | HCID 101984 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(3-Pyridyl)acryloyl chloride hydrochloride | HCID 71360027 | — |
Reaction Steps
Triethylamine (0.5 ml) was added dropwise to a suspension of 3-pyridin-3-ylacrylic acid (5.0 g) in anhydrous dichloromethane (30 ml), and 6 ml of oxalyl chloride was added dropwise slowly in an ice-bath with the temperature no more than 5° C. After addition, the reaction was carried out for 30 min in an ice-bath, and then at room temperature overnight. The completion of reaction was indicated by TLC. The reaction mixture was concentrated under reduced pressure to give a white solid, which was left to stand at room temperature for 1 h, and used directly for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426446B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-8891fb6010e2448e96330da3c46f713f |
| Source note | uspto-grants-2013_04 |