HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338810Generated: October 31, 2026
2-Aminothiophenol → 2-(3-(Benzo[d]thiazol-2-yl)phenoxy)-2-methylpropanoic acid
https://huagongshe.com/reaction/338810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-(3-formylphenoxy)-2-methylpropanoate | HCID 18766496 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3-(Benzo[d]thiazol-2-yl)phenoxy)-2-methylpropanoic acid | HCID 68279296 | 67.7% |
Reaction Steps
In a methanol solvent, a solution including Compound 97b (1.0 eq.) and 2-aminothiophenol (1.0 eq.) was stirred at room temperature for 22 hours. After methanol was evaporated, the residual was purified by silica gel column chromatography using hexane and ethyl acetate (14:1) as a developer. The obtained product was dissolved with 1,4-dioxane, and then, 1 N NaOH (1.5 eq.) was added thereto. The reaction mixture was stirred at room temperature for 17 hours, and 1,4-dioxane was evaporated. The reaction mixture was stirred at room temperature for 17 hours, and 1,4-dioxane was evaporated therefrom. The residual was distributed between ethyl acetate and water, an aqueous layer was acidified with 6 N HCl. The produced precipitate was filtered and washed with water to obtain Compound 120.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889881B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-6773c20cb9f047cc958ef81f86b2c41f |
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| Source note | uspto-grants-2014_11 |
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