HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 12391209, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 2,4-dichloro-alpha-(2,6-dichlorophenyl)benzenepropanoate | HCID 12391182 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 12391209 | HCID 12391209 | — |
Reaction Steps
To a stirred solution of 14.1 parts of methyl 2,4-dichloro-α-(2,6-dichlorophenyl)benzenepropanoate and 6.8 parts of lithium iodide in 120 parts of acetonitrile are added portionwise, during a 5-minutes-period, 2 parts of sodium borohydride. Upon completion, stirring is continued overnight at reflux temperature. The reaction mixture is allowed to cool to room temperature. Then there are added successively 100 parts of a concentrated hydrochloric acid solution (carefully) and after stirring for 30 minutes, 1000 parts of water. The product is extracted twice with 2,2'-oxybispropane. The combined extracts are washed twice with water, dried, filtered and evaporated, yielding 11.2 parts of 2,4-dichloro-β-(2,6-dichlorophenyl)benzenepropanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03991201 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-889e759cdc21447da5984b384fcb766b |
| Source note | uspto-grants-1976_11 |