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Water → 2-(3-hydroxypropyl)phenol

HRID 1650363
Notes
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Reaction equation

HRID 1650363 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[O:7]1[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[CH:11]=[CH:10][CH2:9]C1=O.[OH-:19].[Na+].O>C1COCC1.C(OCC)(=O)C>[OH:7][C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=1[CH2:11][CH2:10][CH2:9][OH:19]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 19595604HCID 19595604, compoundHCID 21226445Aluminium lithium hydride

Product 1

HCID 2667422-(3-hydroxypropyl)phenol

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolvent2×
HCID 8857Ethyl AcetateSolvent

Procedure

To 20 g of lithium aluminum hydride in 200 ml of THF at 0° C. is added dropwise 84 g of 1-benzoxepin-2-one in 200 ml of THF. After addition is complete the reaction mixture is allowed to come to room temperature and stirred 11/4 hours. The reaction 5% of NaOH and 60 ml H2O are sequentially added. The mixture is then diluted with ethyl acetate, acidified and filtered through celite. The EtOAc layer is separated, dried (MgSO4) and concentrated to obtain 3-(-o-hydroxyphenyl)-1-propanol as a brown oil which is used directly in the next step.

Workup

  1. additionAfter addition
  2. customto come to room temperature
  3. additionare sequentially added
  4. filtrationfiltered through celite
  5. customThe EtOAc layer is separated
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-98d0cd13af4a4f6da8f169aa59158525
Source dataset
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04924010

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes