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Diisobutylaluminum hydride → 6-Bromo-1,3-dihydroisobenzofuran-1-ol

HRID 576376
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HRID 576376 반응식
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][O:7][C:8]2=[O:9])=[CH:4][CH:3]=1.CC(C[AlH]CC(C)C)C>ClCCl>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][O:7][CH:8]2[OH:9])=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 2622356-Bromo-1,3-dihydro-2-benzofuran-1-one

생성물 1

HCID 136136836-Bromo-1,3-dihydroisobenzofuran-1-ol수율 96%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
-78 °C

실험 절차

Step 1) To a solution of 6-bromophthalide (144, 550 mg, 2.58 mmol) in dichloromethane (20.0 mL) was slowly added DIBAL-H (2.7 mL, 1.0M solution in hexane) at −78° C., and the reaction mixture was stirred for 1.5 h at −78° C. The resulting mixture was quenched with sat. Na2SO4 and allowed to warm to room temperature. To the mixture was added anhydrous Na2SO4, and the mixture was stirred for 12 h, then filtered and concentrated in vacuo. The crude was purified by silica gel column chromatography to provide 6-bromo-1,3-dihydroisobenzofuran-1-ol (145, 530 mg, 96%) as yellow oil.

후처리

  1. customat −78° C.
  2. customThe resulting mixture was quenched with sat. Na2SO4
  3. temperatureto warm to room temperature
  4. additionTo the mixture was added anhydrous Na2SO4
  5. stirringthe mixture was stirred for 12 h
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe crude was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-5cd40f188d72430b94f3661e01c0cb50
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09034921B2

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