HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 90411212, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (2E)-2-Tetradecenoic acid | HCID 5282738 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90411212 | HCID 90411212 | 99% |
Reaction Steps
(E)-tetradec-2-enoic acid (18.7 g) was dissolved in anhydrous dichloromethane (200 ml) under nitrogen with stirring. The solution was cooled in ice-water bath for 30 min. Oxalyl chloride (9.1 ml) was added dropwise. The reaction mixture was slowly warm up to room temperature overnight. The solvent was removed under vacuum. The product was obtained as clear oil (20.0 g, 99%) and used in next step synthesis without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403760B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-71886ac2884f47f98bee611e78b160d8 |
| Source note | uspto-grants-2016_08 |