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Phosphorus tribromide → Ethyl-3-bromomethyl-4-oxo-3-H-phthalazin-1-ylacetate

HRID 1607982
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반응식

HRID 1607982 반응식
[CH2:1]([O:3][C:4](=[O:19])[CH2:5][C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:9](=[O:16])[N:8]([CH2:17]O)[N:7]=1)[CH3:2].P(Br)(Br)[Br:21]>CCOCC>[CH2:1]([O:3][C:4](=[O:19])[CH2:5][C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:9](=[O:16])[N:8]([CH2:17][Br:21])[N:7]=1)[CH3:2]
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참가 물질

4

반응물 2

HCID 24614Phosphorus tribromideHCID 14519538HCID 14519538, 화합물

생성물 1

HCID 14519540Ethyl-3-bromomethyl-4-oxo-3-H-phthalazin-1-ylacetate수율 60.4%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A solution of ethyl-3-hydroxymethyl-4-oxo-3-H-phthalazin-1-ylacetate (13.1 g), phosphorous tribromide (13.5 g) and anhydrous ether (250 ml) was stirred overnight at room temperature. It was then poured onto water (200 ml). The organic layer was collected, washed again with water (3×100 ml) and then dried over anhydrous sodium sulfate. The dried organic extract was evaporated to dryness and the resulting crude solid was purified by chromatography on silica gel, eluting with 95% CH2Cl2- 5% ethyl acetate (percents by volume) to obtain the title compound (yield: 9.8 g; m.p. 96° C.).

후처리

  1. additionIt was then poured onto water (200 ml)
  2. customThe organic layer was collected
  3. washwashed again with water (3×100 ml)
  4. dry with materialdried over anhydrous sodium sulfate
  5. extractionThe dried organic extract
  6. customwas evaporated to dryness
  7. customthe resulting crude solid was purified by chromatography on silica gel
  8. washeluting with 95% CH2Cl2- 5% ethyl acetate (percents by volume)

출처 및 근거

ORD 기록
ord-7d97ea45a9d24bcca9aa6b9f3d86fd17
출처 데이터셋
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04868301

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