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Water → N-(2-oxo-3-tetrahydrofuranyl)-L-phenylalanine benzyl ester

HRID 2352393
Notes
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Reaction equation

HRID 2352393 reaction equation
C1(C)C=CC(S(O)(=O)=O)=CC=1.[CH2:12]([O:19][C:20](=[O:30])[C@H:21]([CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[NH2:22])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.Br[CH:32]1[CH2:37][CH2:36][O:35][C:33]1=[O:34].C(N(CC)CC)C.O>CN(C)C=O>[CH2:12]([O:19][C:20](=[O:30])[C@H:21]([CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[NH:22][CH:32]1[CH2:37][CH2:36][O:35][C:33]1=[O:34])[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 8471TriethylamineHCID 954632(3H)-Furanone, 3-bromodihydro-HCID 12636207L-phenylalanine benzyl ester p-toluenesulfonate

Product 1

HCID 14819285N-(2-oxo-3-tetrahydrofuranyl)-L-phenylalanine benzyl esterYield 25.8%

Reagents, catalysts & solvents 1

HCID 6228
Dimethylformamide
Solvent

Conditions

Temperature
70 °C

Procedure

Dissolved in 40 ml of dimethylformamide were 8.54 g of L-phenylalanine benzyl ester p-toluenesulfonate and 3.40 g of 2-bromo-γ-butyrolactone. After a dropwise addition of 4.04 g of triethylamine, the resultant mixture was heated and stirred at 70° C. for 18 hours. The reaction mixture was poured into chilled water, followed by extraction with ethyl acetate. The extract was washed successively with water, a 2% aqueous solution of sodium hydrogencarbonate, and water. After drying the extract over anhydrous sodium sulfate, it was distilled under reduced pressure. The residue was isolated and purified by chromatography on a silica gel column (toluene:ethyl acetate=20:1-5:1). From initial fractions of the column effluent, 1.75 g of N-(2-oxo-3-tetrahydrofuranyl)-L-phenylalanine benzyl ester (Isomer A) was obtained as a colorless oily substance.

Workup

  1. additionThe reaction mixture was poured
  2. extractionfollowed by extraction with ethyl acetate
  3. washThe extract was washed successively with water
  4. customAfter drying the
  5. extractionextract over anhydrous sodium sulfate, it
  6. distillationwas distilled under reduced pressure
  7. customThe residue was isolated
  8. custompurified by chromatography on a silica gel column (toluene:ethyl acetate=20:1-5:1)

Sources & evidence

ORD record
ord-2d76e896ead64b699108c49860ddaec5
Source dataset
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04876359

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes