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m-Chloroperbenzoic acid → 5-Bromo-2-methoxyphenol

HRID 54593
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HRID 54593 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH3:11])=[C:6]([CH:9]=1)C=O.ClC1C=C(C=CC=1)C(OO)=[O:17]>C(Cl)(Cl)Cl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH3:11])=[C:6]([OH:17])[CH:9]=1
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 906845-Bromo-2-methoxybenzaldehyde

생성물 1

HCID 1422285-Bromo-2-methoxyphenol수율 96.4%

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

A solution of 5-bromo-2-methoxybenzaldehyde (100 g, 0.46 mol) in CHCl3 (250 ml) was cooled with an ice bath and 3-chloroperoxybenzoic acid (50-60% purity) (146 g, 0.51 mol) in CHCl3 (1000 ml) added. The reaction mixture was allowed to warm slowly to room temperature and stirred for 72h. The white solid was filtered off and the filtrate concentrated in vacuo. The residue was dissolved in Et2O (200 ml) and washed with 1M sodium sulphite solution (2×200 ml) then NaHCO3 [half saturated] (3×200 ml). The ether layer was washed with 10% aqueous NaOH (3×100 ml) and the combined basic extract was acidified with concentrated hydrochloric acid and extracted with Et2O (3×100 ml). The combined organic extract was dried (MgSO4) and florisil (10 g) filtered and the solvent removed under reduced pressure to give the title compound (90 g) as a pate brown solid.

후처리

  1. filtrationThe white solid was filtered off
  2. concentrationthe filtrate concentrated in vacuo
  3. dissolutionThe residue was dissolved in Et2O (200 ml)
  4. washwashed with 1M sodium sulphite solution (2×200 ml)
  5. washThe ether layer was washed with 10% aqueous NaOH (3×100 ml)
  6. extractionthe combined basic extract
  7. extractionextracted with Et2O (3×100 ml)
  8. extractionThe combined organic extract
  9. dry with materialwas dried (MgSO4) and florisil (10 g)
  10. filtrationfiltered
  11. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-3545a78f35774655b3b2b131c75388e2
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05622977

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