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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417114Generated: November 3, 2026

Sodium Hydroxide → HCID 12083248, compound

https://huagongshe.com/reaction/2417114

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 (400 MHz, CDCl3) δ 8.04 (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 numberUS06825222B2
Source datasetuspto-grants-2004_11
ORD IDord-f360a4044fcc415d8910411e71636e27
Source noteuspto-grants-2004_11