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Benzyl Bromide → methyl (2R)-1-benzyl-2-methylazetidine-2-carboxylate

HRID 408580
Notes
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Reaction equation

HRID 408580 reaction equation
[CH3:1][O:2][C:3]([C@@:5]1([CH3:9])[CH2:8][CH2:7][NH:6]1)=[O:4].[CH2:10](Br)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>C1COCC1>[CH3:1][O:2][C:3]([C@@:5]1([CH3:9])[CH2:8][CH2:7][N:6]1[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:4]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7498Benzyl BromideHCID 70556683methyl (2R)-2-methylazetidine-2-carboxylate

Product 1

HCID 44238871methyl (2R)-1-benzyl-2-methylazetidine-2-carboxylate

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
50 °C

Procedure

To a solution of (R)-2-methyl-azetidine-2-carboxylic acid methyl ester (1 eq.) in THF were added TEA (2 eq.) and benzyl bromide (1 eq.). The reaction was heated at 50° C. for 15 h. The solvent was concentrated under reduced pressure, the crude was purified by chromatography on silica gel (elution with heptane/EtOAc 1/0 to 1/1) to afford (R)-1-benzyl-2-methyl-azetidine-2-carboxylic acid methyl ester.

Workup

  1. concentrationThe solvent was concentrated under reduced pressure
  2. customthe crude was purified by chromatography on silica gel (elution with heptane/EtOAc 1/0 to 1/1)

Sources & evidence

ORD record
ord-0cc9d60585034281a0a48241e3e1dfc0
Source dataset
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08759334B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes