HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorophenol → HCID 20164193, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | HCID 20164211 | HCID 20164211 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 20164193 | HCID 20164193 | — |
Reaction Steps
A solution of a p-fluorophenol in t-butanol is treated with one equivalent of potassium t-butoxide, followed by the compound of Example 35A. The reaction mixture is then refluxed until all epoxide has reacted. The reaction is cooled, diluted with water, and extracted with ethyl acetate. The organic extracts are dried and concentrated. The carbobenzyloxy protecting group is removed by standard hydrogenolysis and the final product purified by chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04632929 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-34420be20bb0476986b54249c5407f2f |
| Source note | uspto-grants-1986_12 |