تفاعل #1509623

ord-fc96d62af5724e489b4d962bb7c78dc9

معادلة التفاعل

O=C(c1ccc[nH]1)C(Cl)(Cl)Cl
2-Trichloroacetyl pyrrole
BrBr
bromine
O
water
O=C(c1cc(Br)c[nH]1)C(Cl)(Cl)Cl
title compound 7
المردود 93.8%
O=C(c1cc(Br)c[nH]1)C(Cl)(Cl)Cl
1-(4-bromo-1H-pyrrol-2-yl)-2,2,2-trichloro-ethanone
المردود 93.8%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONOnce addition
  2. 2
    استخلاصextracted with chloroform (3×20 mL) The combined organic layers
  3. 3
    غسيلwere washed with sat. NaHCO3 (2×30 mL), brine (1×20 mL)
  4. 4
    تجفيفdried over anhydrous sodium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    أخرىevaporated to dryness
  7. 7
    أخرىPurification of the residue by column chromatography (Hexanes/Diethyl Ether 95:5)

الإجراء التجريبي

2-Trichloroacetyl pyrrole 6 (5.00 g, 23.3 mmol) was dissolved in anhydrous chloroform (20 mL) The solution was cooled to −10° C. before the drop-wise addition of bromine (1.20 mL, 23.3 mmol) to the flask. Once addition was complete the reaction was allowed to warm to room temperature on its own accord while stirring for an additional 30 minutes. The reaction was poured into water (40 mL) and extracted with chloroform (3×20 mL) The combined organic layers were washed with sat. NaHCO3 (2×30 mL), brine (1×20 mL), dried over anhydrous sodium sulfate, filtered, and evaporated to dryness. Purification of the residue by column chromatography (Hexanes/Diethyl Ether 95:5) yielded the title compound 7 (6.37 g, 93%) as an off-white solid: 1H NMR (300 MHz, DMSO-d6) δ 12.86 (s, 1H), 7.54 (s, 1H), 7.32 (s, 1H); 13C NMR (100 MHz, DMSO-d6) δ 171.67, 129.06, 122.01, 121.54, 97.60, 94.56; HRMS (FAB) calcd for C6H3BrCl3NO (M+) 288.8464, found 288.8479.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08927029B2uspto-grants-2015_01