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Boron tribromide → 1-(3-Hydroxyphenyl)cyclobutane-1-carbonitrile

HRID 1418477
Notes
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Reaction equation

HRID 1418477 reaction equation
[C:1]([C:3]1([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([O:13]C)[CH:8]=2)[CH2:6][CH2:5][CH2:4]1)#[N:2].B(Br)(Br)Br>ClCCl>[C:1]([C:3]1([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([OH:13])[CH:8]=2)[CH2:6][CH2:5][CH2:4]1)#[N:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 25134Boron tribromideHCID 187863241-(3-Methoxyphenyl)cyclobutanecarbonitrile

Product 1

HCID 187863201-(3-Hydroxyphenyl)cyclobutane-1-carbonitrileYield 100%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

To a stirred solution of 1-cyano-1-(3-methoxyphenyl)cyclobutane (1.93 g, 10 mmol) in dry dichloromethane (50 ml) was added a 1.0M solution of boron tribromide in dichloromethane (22 ml, 22 mmol) at 0° C. and the mixture stirred for 30 min at the same temperature, then overnight at room temperature. The reaction mixture was quenched by the addition of water (100 ml) and extracted with dichloromethane (50 ml×2). The organic phase was washed with brine (50 ml), dried (MgSO4) and concentrated in vacuo to afford 1.70 g (100%) of the titled compound as a clear brown oil.

Workup

  1. customovernight
  2. customat room temperature
  3. customThe reaction mixture was quenched by the addition of water (100 ml)
  4. extractionextracted with dichloromethane (50 ml×2)
  5. washThe organic phase was washed with brine (50 ml)
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-34b0babcdd864886bae2c5a235d69bf3
Source dataset
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05883106

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes