HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Amino-5-(4-fluorophenoxy)benzenethiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Amino-6-(4-fluorophenoxy)benzothiazole | HCID 21985512 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-5-(4-fluorophenoxy)benzenethiol | HCID 20063827 | 80.5% |
Reaction Steps
22 g of 2-amino-6-(4-fluorophenoxy)benzothiazole (prepared as described in preparation 7) were added to a mixture of a solution of 90 g of potassium hydroxide in 100 ml of water and 28 ml of ethylene glycol, and the mixture was stirred for 2 hours on an oil bath kept at 130° C under an atmosphere of nitrogen. After the mixture had been cooled to room temperature, 90 ml of acetic acid was added dropwise to the resulting homogenous solution to deposit a precipitate: this was extracted with toluene. The toluene extract was dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure, to afford 16 g of the title compound as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05002942 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-e89974f932284d1380cde5ddab2d870f |
| Source note | uspto-grants-1991_03 |