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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(3-formylphenoxy)-2-methylpropanoateHCID 18766496—
SolventMethanolHCID 887—
Product2-(3-(Benzo[d]thiazol-2-yl)phenoxy)-2-methylpropanoic acidHCID 6827929667.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889881B2
Source datasetuspto-grants-2014_11
ORD IDord-6773c20cb9f047cc958ef81f86b2c41f
Source noteuspto-grants-2014_11