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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229061Generated: November 1, 2026

Sodium Hydroxide → HCID 12083248, compound

https://huagongshe.com/reaction/2229061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 12083247HCID 12083247—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12083248HCID 1208324887%

Reaction Steps

To 2-{4-[2-(2-biphenyl-3-yl-5-methyl-thiazol-4-yl)-ethoxy]-phenoxy}-2-methyl-propionic acid ethyl ester (470 mg, 0.94 mmol) in tetrahydrofuran (10 mL) and methanol (2 mL) was added 2 mL of a 5N NaOH solution. After 24 h, the solution was concentrated in vacuo. The residue was partioned between ethyl acetate and 1N hydrochloric acid. The ethyl acetate layer was dried over magnesium sulfate, filtered and concentrated to afford 385 mg (87% yield) of 2-{4-[2-(2-biphenyl-3-yl-5-methyl-thiazol-4-yl)-ethoxy]-phenoxy}-2-methyl-propionic acid as a white solid. 1H NMR (400MHz, CDCl3) δ8.04 (s, 1H), 7.78 (d, 1H), 7.61-7.55 (m, 3H), 7.45-7.40 (m, 3H), 7.35-7.31 (m, 1H), 6.86-6.82 (m, 2H), 6.79-6.76 (m, 2H), 4.24 (t, 2H), 3.16 (t, 2H), 2.43 (s, 3H), 1.46 (s, 6H). MS EI+(m/e) 474.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417212B1
Source datasetuspto-grants-2002_07
ORD IDord-d3fd3f5771264ad2ad7c8a9dc1fc4812
Source noteuspto-grants-2002_07