HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,3,4-Trifluoro-5chlorobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Chloro-2,3,4-trifluorobenzoyl fluoride | HCID 13565015 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2,3,4-Trifluoro-5chlorobenzyl alcohol | HCID 13565021 | 88.5% |
Reaction Steps
62 g of NaBH4 are initially introduced into 320 ml of dioxane. A solution of 319 g of 5-chloro-2,3,4-trifluorobenzoyl fluoride in 640 ml of dioxane is run into this, at the reflux temperature, over the course of 6 hours. After boiling under reflux for a further hour, the mixture is poured onto ice, the pH is adjusted to 1 with dilute hydrochloric acid, and the organic phase is extracted with methylene chloride and then distilled: 261 g of 2,3,4-trifluoro-5-chlorobenzyl alcohol of boiling point 109° C./12 mbar are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05362909 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-30fd8f6ca4c2474288e10a7464af050d |
| Source note | uspto-grants-1994_11 |