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Methanol → 1-(4-Bromo-2-fluorophenyl)ethan-1-amine

HRID 2371088
Notes
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Reaction equation

HRID 2371088 reaction equation
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([F:10])[CH:3]=1.[CH3:11][Mg]Br.CO.[BH4-].[Na+]>C1COCC1.C(OCC)C>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]([NH2:7])[CH3:11])=[C:4]([F:10])[CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 887MethanolHCID 7360294-Bromo-2-fluorobenzonitrileHCID 4311764Sodium borohydrideHCID 178418573HCID 178418573, compound

Product 1

HCID 185435761-(4-Bromo-2-fluorophenyl)ethan-1-amineYield 44%

Reagents, catalysts & solvents 2

HCID 3283
Diethyl Ether
Solvent
HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
0 °C

Procedure

To a solution of 12 g of 4-bromo-2-fluorobenzonitrile (60 mM) in THF (120 ml) were added 75 ml (150 mM) of a 2 M solution of methylmagnesium bromide in diethyl ether at 0° C. The reaction mixture was stirred at 0° C., for 6 h. Then 200 min of methanol were added gradually to the reaction mixture. Subsequently, 5.7 g (150 mM) of sodium borohydride were added in portions, and the mixture was stirred at room temperature for 16 h. Thereafter, the reaction mixture was concentrated under reduced pressure, and 200 ml of water were added. The pH was adjusted to pH=˜1 with 2 M HCl, and the aqueous solution was extracted with chloroform. Subsequently, the pH was adjusted to pH=˜9 with 2M NaOH, and extraction was effected with chloroform (2×100 ml). The combined chloroform extracts were dried, and the solvent was removed under reduced pressure. 73 g (44%) of 1-(4-bromo-2-fluorophenyl)ethanamine were obtained as a yellow oil.

Workup

  1. stirringthe mixture was stirred at room temperature for 16 h
  2. concentrationThereafter, the reaction mixture was concentrated under reduced pressure, and 200 ml of water
  3. additionwere added
  4. extractionthe aqueous solution was extracted with chloroform
  5. extractionSubsequently, the pH was adjusted to pH=˜9 with 2M NaOH, and extraction
  6. dry with materialThe combined chloroform extracts were dried
  7. customthe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-29d17286995745748a3b1a4a541d58c1
Source dataset
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08710242B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes