HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 178484892, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178484893 | HCID 178484893 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178484892 | HCID 178484892 | — |
Reaction Steps
To a solution of 38.1 g. (0.1 moles) of N1 -methyl-N2 -(4-bromo-3-trifluoromethylphenyl)-2-acetoxy isobutyramidine in 500 ml. of ethanol, add 5.6 g. (0.1 moles) of potassium hydroxide, maintaining the reaction at room temperature. Stir at room temperature for several hours (until there is no evidence of starting ester by tlc). Remove the solvent in vacuo, partition the residue between ether and water, dry the ether extract over sodium sulfate, filter, and precipitate the product of this reaction as its hydrochloride salt, by adding 25 ml. of 4.0N ethereal hydrogen chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03965176 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-38e41d60eb474eb5bb593ef66fa5ea71 |
| Source note | uspto-grants-1976_06 |