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Water → HCID 68620118, compound

HRID 1433766
Notes
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Reaction equation

HRID 1433766 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([NH:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[C:9]([OH:11])=[O:10])=[CH:4][CH:3]=1.C(=O)([O-])O.[K+].[CH2:25](Br)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.O>CN(C)C=O>[CH2:25]([O:10][C:9](=[O:11])[CH:8]([C:5]1[CH:4]=[CH:3][C:2]([Br:1])=[CH:7][CH:6]=1)[NH:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 7498Benzyl BromideHCID 516893Potassium BicarbonateHCID 223091702-(4-Bromophenyl)-2-{[(tert-butoxy)carbonyl]amino}acetic acid

Product 1

HCID 68620118HCID 68620118, compoundYield 50%

Reagents, catalysts & solvents 1

HCID 6228
Dimethylformamide
Solvent

Procedure

(4-Bromo-phenyl)-tert-butoxycarbonylamino-acetic acid (780 mg, 2.4 mmol) was dissolved in N,N-dimethylformamide (15 mL) and to this was added potassium hydrogen carbonate (260 mg, 2.6 mmol) followed by benzyl bromide (281 μL, 2.4 mmol) and stirring continued at ambient temperature for 6 hours. The reaction was poured into water (50 mL) and extracted with ethyl acetate (2×60 mL). The organic extracts were washed with water (2×20 mL), brine, dried over sodium sulfate and filtered through a layer of silica gel. The filtrate was concentrated in vacuo and the residue crystallized from 100% hexane to give (4-bromo-phenyl)-tert-butoxycarbonylamino-acetic acid benzyl ester (500 mg, 50%).

Workup

  1. extractionextracted with ethyl acetate (2×60 mL)
  2. washThe organic extracts were washed with water (2×20 mL), brine
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered through a layer of silica gel
  5. concentrationThe filtrate was concentrated in vacuo
  6. customthe residue crystallized from 100% hexane

Sources & evidence

ORD record
ord-00c19038f89a4cc9ac96c4aa5b2c1c8d
Source dataset
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07612212B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes