تفاعل #57918

معادلة التفاعل

(4-{3-[1-(4-tert-butyl-phenyl)-ethylideneaminooxy]-propoxy}-phenyl)-acetic acid methyl ester

sodium hydroxide

→

title compound

المردود 46.0%

(4-{3-[1-(4-tert-Butyl-phenyl)-ethylideneaminooxy]-propoxy}-phenyl)-acetic Acid

المردود 46.0%

المذيبات

tetrahydrofuran ethanol

ظروف التفاعل

المعالجة

1. 1
   تركيزIt was concentrated to a small volume
2. 2
   استخلاصextracted with ethyl acetate
3. 3
   غسيلThe combined organics were washed with brine
4. 4
   تجفيفdried over anhydrous magnesium sulfate
5. 5
   تركيزconcentrated in vacuo
6. 6
   أخرىThe residue was purified by flash chromatography

الإجراء التجريبي

To a solution of (4-{3-[1-(4-tert-butyl-phenyl)-ethylideneaminooxy]-propoxy}-phenyl)-acetic acid methyl ester (3.55 mmol) in tetrahydrofuran/ethanol (3/2) (20 mL) was added 1 M sodium hydroxide solution (6 mL, 6 mmol) and the reaction was stirred overnight at room temperature. It was concentrated to a small volume, acidified to pH 1 with 1M hydrochloric acid solution and extracted with ethyl acetate. The combined organics were washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by flash chromatography using ethyl acetate/hexanes (20/80)+1% formic acid to afford the title compound (0.620 g, 46%) as a light yellow solid. mp=98.7-99.7° C.; mass spectrum (−ESI, M−H) m/z 382. 1H NMR (400 MHz, DMSO-d6); δ 12.20 (bs, 1H), 7.55 (d, 2H), 7.38 (d, 2H). 7.14 (d, 2H), 6.87 (d, 2H), 4.25 (t, 2H), 4.05 (t, 2H), 3.47 (s, 2H), 2.16 (s, 3H), 2.09 (m, 2H), 1.25 (s, 9H). Elemental analysis: Calcd. for C23H29NO4: C, 72.04; H, 7.62; N, 3.65, Found: C, 71.43; H, 7.87; N, 3.52.

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