Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13391436 | HCID 13391436 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13391440 | HCID 13391440 | — |
Reaction Steps
15 g (0.126 mol) of thionyl chloride were added dropwise to a stirred solution of 19.7 g (0.05 mol) of the R enantiomer of 2-[3-(2,6-dichloro-4-trifluoromethylphenoxy)-phenoxy]-propionic acid in 100 ml of toluene at 20° C. The mixture was heated to 100° C. for 2 hours. Thereafter, the reaction mixture was evaporated down by stripping off the volatile constituents under reduced pressure. In this manner, the R enantiomer of 2-[3-(2,6-dichloro-4-trifluoromethyl-phenoxy)-phenoxy]-propionic acid-chloride was obtained in the form of an oily product, which was used for the further reaction. ##STR37##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04622415 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-2c5154ba1e06467682b3ab346571c230 |
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| Source note | uspto-grants-1986_11 |
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