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1-(4-Bromo-2-nitro-phenoxy)-cyclopropanecarboxylic acid ethyl ester → 6-bromospiro[benzo[b][1,4]oxazine-2,1'-cyclopropan]-3(4H)-one

HRID 72590
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HRID 72590 반응식
C([O:3][C:4]([C:6]1([O:9][C:10]2[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][C:11]=2[N+:17]([O-])=O)[CH2:8][CH2:7]1)=O)C>C(O)(=O)C.C(OCC)(=O)C.[Fe]>[Br:16][C:13]1[CH:14]=[CH:15][C:10]2[O:9][C:6]3([CH2:8][CH2:7]3)[C:4](=[O:3])[NH:17][C:11]=2[CH:12]=1
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참가 물질

5

반응물 1

HCID 583407841-(4-Bromo-2-nitro-phenoxy)-cyclopropanecarboxylic acid ethyl ester

생성물 1

HCID 215813596-bromospiro[benzo[b][1,4]oxazine-2,1'-cyclopropan]-3(4H)-one수율 93.2%

시약·촉매·용매 3

HCID 23925Iron촉매HCID 176Acetic Acid용매HCID 8857Ethyl Acetate용매

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온도
60 °C

실험 절차

To a stirred solution of 1-(4-bromo-2-nitro-phenoxy)-cyclopropanecarboxylic acid ethyl ester (3.5 g, 10.6 mmol) in glacial acetic acid (40 mL) was added iron powder (5.9 g, 106.1 mmol) at room temperature and the reaction mixture was heated at 60° C. for 3 h. The mixture was cooled to room temperature, diluted with ethyl acetate, and filtered through celite bed. The filtrate was concentrated, and the resulting residue was taken in ethyl acetate and washed with water and saturated sodium bicarbonate solution, then the organic layer was dried over sodium sulfate, concentrated and the resulting residue was purified by silica gel column chromatography to furnish 6-bromospiro[4H-1,4-benzoxazine-2,1′-cyclopropane]-3-one (2.51 g).

후처리

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationfiltered through celite bed
  3. concentrationThe filtrate was concentrated
  4. washwashed with water and saturated sodium bicarbonate solution
  5. dry with materialthe organic layer was dried over sodium sulfate
  6. concentrationconcentrated
  7. customthe resulting residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-e16354d863254b13bbe38b3bea4cb0e0
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08828951B2

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