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

HRID 576376
Notes
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Reaction equation

HRID 576376 reaction equation
[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
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Conditions

Temperature
-78 °C

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-5cd40f188d72430b94f3661e01c0cb50
Source dataset
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09034921B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes