تفاعل #1960519

ord-b3a6352071c1492f8d60f1fcf93a3c65

معادلة التفاعل

COC(=O)C(C)c1ccc2cc(O)ccc2c1
2-(6-hydroxy-naphthalen-2-yl)-propionic acid methyl ester
c1ccncc1
pyridine
O=C(Cl)CBr
bromoacetyl chloride
COC(=O)C(C)c1ccc2cc(OC(=O)CBr)ccc2c1
2-[6-(2-bromo-acetoxy)-naphthalen-2-yl]-propionic acid methyl ester
المردود 45.9%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThe reaction mixture was washed with water (500 ml) and 5% solution of sodium carbonate
  2. 2
    تجفيفby drying over sodium sulphate and distillation
  3. 3
    أخرىto get crude compound, which
  4. 4
    أخرىwas purified by column chromatography

الإجراء التجريبي

To a solution of 2-(6-hydroxy-naphthalen-2-yl)-propionic acid methyl ester (20 grams) and pyridine (10.3 grams) in dichloromethane (200 ml) maintained at 0-5° C. under N2 atmosphere was added dropwise bromoacetyl chloride (19.6 grams). The reaction was stirred at the same temperature for one hour. The reaction mixture was washed with water (500 ml) and 5% solution of sodium carbonate followed by drying over sodium sulphate and distillation to get crude compound, which was purified by column chromatography using hexane as eluant to get pure 2-[6-(2-bromo-acetoxy)-naphthalen-2-yl]-propionic acid methyl ester (14 grams) as a dark brown syrup. The pure product was characterized using 1H NMR spectroscopy in CDCl3 δ 1.55 (d, 3H, CH3), 3.65 (s, 3H, Ester), 3.82 (q, 1H, CH), 4.08 (s, 2H, OCH2) 7.20 (dd, 1H, Ar), 7.4 (dd, 1H, Ar), 7.57 (d, 1H, Ar), 7.72 (d, 1H, Ar), 7.78 (d, 1H, Ar), 7.84 (d, 1H, Ar).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08303978B2uspto-grants-2012_11