2,6-Dimethylaniline → Glycine, N-(2,6-dimethylphenyl)-

HRID 491379Notes

Reaction equation

HRID 491379 reaction equation
CC1C=CC=C(C)C=1N.BrCC(OCC)=O.Br.[CH3:18][C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([CH3:25])[C:20]=1[NH:26][CH2:27][C:28]([OH:30])=[O:29]>ClCCl>[CH3:25][C:21]1[CH:22]=[CH:23][CH:24]=[C:19]([CH3:18])[C:20]=1[NH:26][CH2:27][C:28]([OH:30])=[O:29]

Participants

5

Reactant 3

HCID 68962,6-DimethylanilineHCID 7748Ethyl bromoacetateHCID 21879725HCID 21879725, compound

Product 1

HCID 826274Glycine, N-(2,6-dimethylphenyl)-

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

2,6-Dimethylaniline (6.1 g, 50.4 mmol), and ethyl bromoacetate (8.4 g, 50.4 mmol) were refluxed neat for 10 min. The reaction mixture was cooled to room temperature and poured into dichloromethane (75 mL). A precipitated formed which was collected and triturated which dichloromethane (25 mL). N-(2,6-Dimethylphenyl)glycine hydrobromide salt (1.21 g, 4.6 mmol, 9.0%) was collected as a white crystalline solid. 1H NMR (CD3OD) d 2.48 (s, 6H), 4.29 (s, 2H), 7.00-7.10 (m, 3H).

Workup

  1. customA precipitated
  2. customformed which
  3. customwas collected
  4. customtriturated which dichloromethane (25 mL)

Sources & evidence

ORD record
ord-b3709b11fa384151bbf3b53b527d2132
Source dataset
uspto-grants-2009_05
Patent number
US07531538B2

Reaction notes

Loading…