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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417066Generated: November 1, 2026

Sodium Hydroxide → HCID 22633474, compound

https://huagongshe.com/reaction/2417066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69871815HCID 69871815—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22633474HCID 22633474—

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of 2-{4-[2-(2-biphenyl-4-yl-5-methyloxazol-4-yl)-ethoxy]-2-methylphenoxy}-2-methylpropionic acid ethyl ester (11.8 mmol) in THF (30 mL) and methanol (60 mL) was treated with 5N aqueous NaOH (20 mL). The solution was heated at 55° C. for 1 h, cooled to ambient temperature, and concentrated in vacuo. The residue was treated with ice water (20 mL), acidified with 5N aqueous HCl (25 mL), and extracted with ethyl acetate (200 mL). The organic layer was washed with brine (40 mL), dried (Na2SO4), and concentrated to yield the desired product. mp 122-123° C.; 1H NMR (400 MHz, CDCl3) δ 8.07 (d, J=8.8 Hz, 2H), 7.67 (d, J=8.8 Hz, 2H), 7.62 (dt, J=6.8, 1.2 Hz, 2H), 7.45 (tt, J=6.8, 1.2 Hz, 2H), 7.37 (tt, J=7.2, 2.0 Hz, 1H), 6.82 (d, J=8.8 Hz, 1H), 6.71 (d, J=3.2 Hz, 1H), 6.57 (dd, J=8.8, 3.2 Hz, 1H), 4.16 (t, J=6.4 Hz, 2H), 3.82 (t, J=6.4 Hz, 2H), 2.40 (s, 3H), 2.21 (s, 3H), 1.56 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825222B2
Source datasetuspto-grants-2004_11
ORD IDord-6246e8dcb0a04d55ba4b8472d03eea28
Source noteuspto-grants-2004_11