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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898467Generated: October 30, 2026

Sodium Hydroxide → HCID 22261210, compound

https://huagongshe.com/reaction/898467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69310455HCID 69310455—
SolventEthanolHCID 702—
ProductHCID 22261210HCID 2226121082.8%

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of {3-ethyl-4-[2-(5-methyl-2-phenyloxazol-4-yl)ethoxy]phenoxy}acetic acid ethyl ester (0.23 g, 0.57 mmol) in ethanol (10 mL) was treated with 2.5 N aqueous NaOH (1.1 mL), and heated at 55° C. for 2 h. The reaction was cooled to ambient temperature and concentrated down to near dryness. The residue was then diluted with EtOAc (40 mL) and water (20 mL) and acidified to pH=1 with 1N aqueous HCl. The organic layer was washed with brine (20 mL), dried (Na2SO4) and concentrated in vacuo to give a white solid (0.18 g, 81%). 1H NMR (400 MHz, CDCl3) δ 7.98 (dd, J=7.8, 2.9 Hz, 2H), 7.46-7.40 (m, 3H), 6.79 (d, J=2.9 Hz, 1H), 6.70 (d, J=8.8 Hz, 1H), 6.63 (dd, J=8.8, 2.9 Hz, 1H), 4.58 (s, 2H), 4.14 (t, J=6.4 Hz, 2H), 3.01 (t, J=6.4 Hz, 2H), 2.56 (q, J=7.5 Hz, 2H), 2.39 (s, 3H), 1.11 (t, J=7.6 Hz, 3H); MS (ES) m/e 382 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351728B2
Source datasetuspto-grants-2008_04
ORD IDord-0343542b7eb74c9ebb6863baa5d747ff
Source noteuspto-grants-2008_04