반응 #48452

ord-6738cf681934443c87d9132a53ea6f01

반응 방정식

COCCBr
2-bromoethyl methyl ether
O=C([O-])[O-].[Cs+].[Cs+]
Cesium carbonate
O=[N+]([O-])c1cc(Br)cnc1O
5-bromo-3-nitropyridin-2-ol
COCCBr
2-bromoethyl methyl ether
O
water
COCCn1cc(Br)cc([N+](=O)[O-])c1=O
title compound
수율 58.4%
COCCn1cc(Br)cc([N+](=O)[O-])c1=O
5-Bromo-1-(2-methoxyethyl)-3-nitropyridin-2(1H)-one
수율 58.4%

반응 조건

온도
60°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITAfter 4 h
  2. 2
    추출The mixture was extracted with ethyl acetate (3×)
  3. 3
    세척the combined organic extracts were washed with saturated brine
  4. 4
    건조dried over sodium sulfate
  5. 5
    여과filtered
  6. 6
    농축concentrated
  7. 7
    기타Purification by silica gel chromatography (100% hexanes→40% ethyl acetate/hexanes)

실험 절차

Cesium carbonate (14.88 g, 45.66 mmol) was added to a solution of 5-bromo-3-nitropyridin-2-ol (10.0 g, 45.7 mmol) and 2-bromoethyl methyl ether (4.29 mL, 45.66 mmol) in N,N-dimethylformamide (400 mL). After 3 h, additional 2-bromoethyl methyl ether (4.29 mL, 45.7 mmol) was added, and the reaction was heated to 60° C. After 4 h, water was added. The mixture was extracted with ethyl acetate (3×), and the combined organic extracts were washed with saturated brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→40% ethyl acetate/hexanes) gave the title compound (7.39 g). MS 277 (M).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745427B2uspto-grants-2010_06