HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Trifluoromethyl)phenol → 2-Butanol, 1-[3-(trifluoromethyl)phenoxy]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Trifluoromethyl)phenol | HCID 7376 | — |
| Reactant | 1,2-Epoxybutane | HCID 7834 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Butanol, 1-[3-(trifluoromethyl)phenoxy]- | HCID 11379302 | — |
Reaction Steps
In a bomb tube (pressurized vessel), 40.5 g of 3-hydroxybenzotrifluoride, 18.0 g of α-butylene oxide and 1.0 g of lithium hydroxide monohydrate are heated for 16 hours at 140° C. After the reaction vessel has cooled, the reaction mixture is dissolved in 200 ml of ethyl acetate, and the organic phase is washed with water and subsequently dried over sodium sulfate. After concentration, the desired product 1-(3-trifluoromethylphenoxy)-2-butanol is obtained in a yield of 54.0 g and in high purity. The product can be employed in the subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05831114 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-987c0c0333174d99907148f34b8c1d7b |
| Source note | uspto-grants-1998_11 |