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Ethylenediaminetetraacetic Acid → 4-[5-(1-Imidazolylmethyl)-thien-2-yl]-4-oxo-butyric acid methyl ester

HRID 2164394
Notes
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Reaction equation

HRID 2164394 reaction equation
[Cl-].[CH3:2][O:3][C:4](=[O:10])[CH2:5][CH2:6][C:7](O)=[O:8].[S:11]1[CH:15]=[CH:14][CH:13]=[C:12]1[CH2:16]N1C=CN=C1.[Cl-].[Al+3].[Cl-].[Cl-].[CH2:26]([N:37]([CH2:42]C(O)=O)CC(O)=O)[CH2:27][N:28](CC(O)=O)CC(O)=O.[OH-].[Na+]>ClCCCl>[CH3:2][O:3][C:4](=[O:10])[CH2:5][CH2:6][C:7]([C:15]1[S:11][C:12]([CH2:16][C:42]2[NH:37][CH:26]=[CH:27][N:28]=2)=[CH:13][CH:14]=1)=[O:8]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 6049Ethylenediaminetetraacetic AcidHCID 14798Sodium HydroxideHCID 6451240Aluminum(III) ChlorideHCID 13120569HCID 13120569, compoundHCID 86605420Succinic acid methylester chloride

Product 1

HCID 704876864-[5-(1-Imidazolylmethyl)-thien-2-yl]-4-oxo-butyric acid methyl ester

Reagents, catalysts & solvents 1

HCID 111,2-DichloroethaneSolvent2×

Conditions

Temperature
50 °C

Procedure

19.5 g of succinic acid methyl ester chloride and then a solution of 20 g of 1-(thien-2-ylmethyl)-imidazole in 200 ml of 1,2-dichloroethane are added dropwise to a suspension of 53.5 g of aluminium chloride in 240 ml of 1,2-dichloroethane, whilst cooling with ice. The mixture is then stirred at 50° C. for 3 hours. After it has been cooled, the reaction mixture is stirred into a mixture of 147.3 g of ethylenediaminetetraacetic acid and 500 g of ice and is brought to about pH 8 by addition of dilute sodium hydroxide solution. The phases are separated and the organic phase is dried over Na2SO4 and concentrated. Extraction of the residue by stirring with hexane gives colourless crystals.

Workup

  1. temperaturewhilst cooling with ice
  2. temperatureAfter it has been cooled
  3. customThe phases are separated
  4. dry with materialthe organic phase is dried over Na2SO4
  5. concentrationconcentrated
  6. extractionExtraction of the residue
  7. stirringby stirring with hexane
  8. customgives colourless crystals

Sources & evidence

ORD record
ord-1e702003e50c4be8b22fd604509cb481
Source dataset
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04504479

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes