HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Allyl chlorodifluoroacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Chlorodifluoroacetic acid | HCID 66154 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Allyl chlorodifluoroacetate | HCID 10012339 | — |
Reaction Steps
In a 1.5 liter sulfonation flask with a water separator, 294.0 g (2.25 mol) of chlorodifluoroacetic acid (pure, from Fluka AG) and 228.0 g (3.93 mol) of allyl alcohol are dissolved in 1 liter of chloroform and kept under reflux for 17 hours in the presence of 11.25 g of p-toluenesulfonic acid (0.06 mol), 41 ml of H2O separating out. The yellow reaction solution is washed twice with H2O and 3 times with saturated aqueous NaHCO3 solution, dried over MgSO4 and distilled under normal pressure through a Vigreux column. Yield: 306.0 g (80%) of a colourless oil of boiling point 98°-100° C./988 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892962 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-72a6fd8c9a07476bb8fa95545f96406d |
| Source note | uspto-grants-1990_01 |