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Phenethylamine → Methyl 2-(phenethylamino)acetate

HRID 1198071
Notes
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Reaction equation

HRID 1198071 reaction equation
[C:1]1([CH2:7][CH2:8][NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[CH2:11][C:12]([O:14][CH3:15])=[O:13]>C1(C)C=CC=CC=1>[C:1]1([CH2:7][CH2:8][NH:9][CH2:11][C:12]([O:14][CH3:15])=[O:13])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 1001PhenethylamineHCID 60984Methyl bromoacetate

Product 1

HCID 22991956Methyl 2-(phenethylamino)acetateYield 124.2%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

To a stirred solution of 2-phenylethylamine (9.68 g, 40 mmol) in toluene (50 mL) was added methyl bromoacetate (6.12 g, 20 mmol) dropwise at room temperature and was left stirring for 18 hours. The reaction mixture was filtered before removing the solvent in vacuo and the residue was purified by chromatography over silica gel to yield 4.8 g (61%) of the title compound as an oil. NMR (250 MHz, CDCl3) δ (1H, s), 2.92 (4H, m), 3.43 (2H, s), 3.71 (2H, s), 7.27 (5H, m).

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. waitwas left
  2. filtrationThe reaction mixture was filtered
  3. custombefore removing the solvent in vacuo
  4. customthe residue was purified by chromatography over silica gel

Sources & evidence

ORD record
ord-58b2afecc5d94c0eaaacd595f2a7de3b
Source dataset
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05278316

Reaction notes

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