HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 16-Hexadecanoyloxyhexadecanoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 16-Hexadecanoyloxyhexadecanoic acid | HCID 19606746 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 16-Hexadecanoyloxyhexadecanoyl chloride | HCID 21711984 | 100% |
Reaction Steps
16-Hexadecanoyloxyhexadecanoic acid (7.73 g, 15.13 mmol) prepared as in (c) above was dissolved in tetrahydrofuran (140 ml) and oxalyl chloride (4.80 g, 37.83 mmol) was added dropwise. The mixture was stirred at room temperature for 3 days and then the solvent and unreacted oxalyl chloride were evaporated under reduced pressure to give 8.0 g (100%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990263 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-9fc4cc17c55d41b1a521b374511dd0e5 |
| Source note | uspto-grants-1999_11 |