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Water ethanol → 2-Formylamino-3-hydroxy-4-ethyl-4-pentenoic acid ethyl ester

HRID 728861
Notes
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Reaction equation

HRID 728861 reaction equation
[CH2:1]([O:3][C:4]([CH:6]1[CH:10]([C:11]([CH2:13][CH3:14])=[CH2:12])[O:9][CH:8]=[N:7]1)=[O:5])[CH3:2].C([OH:17])C.O>>[CH2:1]([O:3][C:4](=[O:5])[CH:6]([NH:7][CH:8]=[O:17])[CH:10]([OH:9])[C:11]([CH2:13][CH3:14])=[CH2:12])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 19096565Water ethanolHCID 542119745-(Buten-2-yl)-2-oxazoline-4-carboxylic acid ethyl ester

Product 1

HCID 216672992-Formylamino-3-hydroxy-4-ethyl-4-pentenoic acid ethyl ester

Procedure

The starting material is manufactured as follows: Reaction of 2-methylene-butyraldehyde with isocyanoacetic acid ethyl ester in a manneranalogous to that described in Example 1 yields 5-(buten-2-yl)-2-oxazoline-4-carboxylic acid ethyl ester. A solution of 16g of 5-(buten-2-yl)-2-oxazoline-4-carboxylic acid ethyl ester in 100 ml of ethanol/water (1:1) is heated at the boil, under reflux, for 15 hours. Thewhole is concentrated by evaporation in vacuo, the residue is taken up in 200 ml of dichloromethane, dried over sodium sulphate and filtered, and the filtrate is concentrated by evaporation to yield 2-formylamino-3-hydroxy-4-ethyl-4-pentenoic acid ethyl ester.

Workup

temperature
under reflux, for 15 hours
  • concentrationThewhole is concentrated by evaporation in vacuo
  • dry with materialdried over sodium sulphate
  • filtrationfiltered
  • concentrationthe filtrate is concentrated by evaporation
  • Sources & evidence

    ORD record
    ord-c2157a93a0cb48af8d537b462539cfec
    Source dataset
    uspto-grants-1991_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05051413

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes