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m-Chloroperbenzoic acid → 2,3-Dihydro-1,4-benzodioxin-6-ol

HRID 38381
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HRID 38381 반응식
[O:1]1[C:6]2[CH:7]=[CH:8][C:9](C=O)=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1.C1C=C(Cl)C=C(C(OO)=[O:21])C=1.C([O-])(O)=O.[Na+]>C(Cl)Cl>[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([OH:21])=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1
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참가 물질

5

반응물 3

HCID 70297m-Chloroperbenzoic acidHCID 2481272,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 516892Sodium Bicarbonate

생성물 1

HCID 91152732,3-Dihydro-1,4-benzodioxin-6-ol수율 96.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
50 °C

실험 절차

To a solution of 2,3-dihydro-benzo[1,4]dioxin-6-carboxaldehyde (30.0 g, 183 mmol) in 500 ml CH2Cl2 was added mCPBA (37.85 g, 219 mmol). The suspension was heated to 50° C. After 16 h saturated NaHCO3 was added and the mixture was extracted with CH2Cl2 The combined organics were concentrated in vacuo and taken up in MeOH and 200 ml 4M NaOH was added. After 2 h the mixture was acidified with 4M HCl and extracted with ethyl acetate. The combined organics were washed with saturated NaHCO3, washed with brine, concentrated in vacuo, and taken up in CH2Cl2. The solution was filtered to remove the precipitate. The resulting solution was stirred with saturated NaHCO3 for 1 h, separated, dried over MgSO4, filtered and concentrated in vacuo to give 2,3-dihydro-benzo[1,4]dioxin-6-ol (26.92 g, 94%).

후처리

  1. extractionthe mixture was extracted with CH2Cl2 The combined
  2. concentrationorganics were concentrated in vacuo
  3. addition200 ml 4M NaOH was added
  4. extractionextracted with ethyl acetate
  5. washThe combined organics were washed with saturated NaHCO3
  6. washwashed with brine
  7. concentrationconcentrated in vacuo
  8. filtrationThe solution was filtered
  9. customto remove the precipitate
  10. customseparated
  11. dry with materialdried over MgSO4
  12. filtrationfiltered
  13. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-14d17fc460f14beea1aad9fb14bea198
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524725B2

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