Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Lauric Acid | HCID 3893 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | Dodecanoyl chloride | HCID 8166 | 97.1% |
Reaction Steps
To a stirred mass of lauric acid (200 g, 0.999 gmol) and sodium N-lauroyl, N-methyl taurate (0.6 g, 0.0017 gmol) at 25° C. under nitrogen blanket, thionyl chloride (123 g, 1.03 gmol) was added slowly at 25° C. and atmospheric pressure over a period of 2 hours maintaining temperature below 25° C. The hydrochloric acid and sulfur dioxide generated during the process was continuously scrubbed in a gas scrubber containing caustic lye. The reaction mixture was stirred for additional 4 hours at the reaction temperature. The progress of reaction in the last phase was monitored by measuring alkanoyl chloride formation. Nitrogen gas was purged through the reaction mass for 3 hours to remove the residual traces of sulfur dioxide, hydrogen chloride gas and unreacted thionyl chloride. At the end of this procedure lauroyl chloride (212 g, 97%) was obtained as practically colorless product. The detailed analysis is given in the Table 13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09187407B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-fa57391c33474d98b9003a55e1b38279 |
|---|
| Source note | uspto-grants-2015_11 |
|---|