تفاعل #79745

ord-c1d2dc2209614685a7c4ac39f3fb5372

معادلة التفاعل

CCOC(=O)CBr
ethyl bromoacetate
COc1cccc2[nH]ccc12
4-methoxyindole
[Li][CH2]CCC
n-butyl lithium
CCOC(=O)Cc1c[nH]c2cccc(OC)c12
ethyl [4-methoxyindol-3-yl]acetate

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe cooling bath was removed
  2. 2
    غسيلwashed with water
  3. 3
    غسيلwashed with brine
  4. 4
    تجفيفdried over sodium sulfate
  5. 5
    أخرىevaporated in vacuo
  6. 6
    أخرىThe residue was chromatographed on silica gel eluting with a gradient hexane/10-50% ethyl ether
  7. 7
    أخرىto give

الإجراء التجريبي

To a solution of 2.94 gm (20 mmol) of 4-methoxyindole in 150 ml of tetrahydrofuran was added slowly 13 ml of n-butyl lithium (1.6M in hexane; 20 mmol) followed by the slow addition of 20 ml of zinc chloride (1.0M in ethyl ether; 20 mmol) at 0-5° C. The cooling bath was removed and the solution stirred for 2 hours and then treated with 2.1 ml (25 mmol) of ethyl bromoacetate for 19 hours, diluted with ethyl acetate, washed with water, washed with brine, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel eluting with a gradient hexane/10-50% ethyl ether to give starting material (40%) and then product, 2.3 gm, 50%, as an oil. 1H NMR (CDCl3) δ: 1.25 (t, 3H), 3.85 (s, 3H), 3.90 (s, 2H), 4.10 (q, 2H), 6.45 (d, 1H), 6.90 (d, 1H), 6.95 (s, 1H), 7.05 (t, 1H), 8.00 (br s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06713645B1uspto-grants-2004_03