HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044047Generated: October 26, 2026
Hydrochloric Acid → Phenyl-o-methylphenylamino-acetic acid hydrochloride
https://huagongshe.com/reaction/1044047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl bromophenylacetate | HCID 97780 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Phenyl-o-methylphenylamino-acetic acid hydrochloride | HCID 67124826 | 63% |
Reaction Steps
Ethyl 2-bromo-2-phenylacetate (0.28 ml, 1.64 mmol), ortho-toluidine (0.26 ml, 2.47 mmol), and DIPEA (0.43 ml, 2.47 mmol) were dissolved in acetonitrile (5 ml) and stirred under microwave irradiation at 100° C. for 1 hours (Conversion complete by UPLC/MS-UV). Lithium hydroxide hydrate (207 mg, 4.94 mmol) and water (3 ml) were added, and the mixture was stirred at room temperature for 16 hours. 4M HCl in dioxane was added until pH was about 1, then the solvents were evaporated, the residue was suspended in water, sonicated, and cooled at 0° C., and the resulting solid was recovered by filtration and dried under vacuum to get intermediate I22 (290 mg, 63% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563577B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-a83dc8177a004444a34cbdb499ebd8f1 |
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| Source note | uspto-grants-2013_10 |
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