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Chloride → 4-Carbomethoxymethyl azetidin-2-one

HRID 355178
Notes
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Reaction equation

HRID 355178 reaction equation
[Cl-].[Si]([N:9]1[C@H:12]([CH2:13][C:14](SC)(SC)SC)[C@@H:11]([C@H](O)C)[C:10]1=[O:24])(C(C)(C)C)(C)C.[C:25](=O)(O)[O-:26].[Na+].C[OH:31]>>[C:14]([CH2:13][CH:12]1[NH:9][C:10](=[O:24])[CH2:11]1)([O:26][CH3:25])=[O:31]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 312ChlorideHCID 887MethanolHCID 516892Sodium BicarbonateHCID 13104625(3S,4R)-1-(t-butyldimethylsilyl)3-[(R)-1-hydroxyethyl]-4-[2,2,2-tri(methylthio)ethyl]azetidin-2-one

Product 1

HCID 128327374-Carbomethoxymethyl azetidin-2-one

Conditions

Temperature
0 °C

Procedure

Mecuric chloride (12.37 g, 45.6 mmol) is added in one portion to a solution of (3S,4R)-1-(t-butyldimethylsilyl)-3-[(R)-1-hydroxyethyl]-4-[2,2,2-tri(methylthio)-ethyl]azetidin-2-one (6.0 g, 15.2 mmol) in 250 ml of absolute methanol at 0° C. The resulting mixture (heavy white precipitate) is stirred at 0° C. for 3 min., then quenched by addition of sodium bicarbonate (8.99 g, 107 mmol). This mixture is then filtered and the solid residue is washed with additional methanol. The combined filtrate and washings are concentrated in vacuo and the residue is partitioned between ethyl acetate and saturated aqueous ammonium chloride solution. The organic phase is separated, washed with saturated aqueous ammonium chloride solution, water and brine and dried over magnesium sulfate. Removal of solvents in vacuo gives an oil which is chromatographed on a silica gel column (3:2 cyclohexane:ethyl acetate) to yield (3S,4R)-1-(t-butyldimethylsilyl)-3-[(R)-1-hydroxyethyl)]-4-carbomethoxymethyl azetidin-2-one.

Workup

  1. filtrationThis mixture is then filtered
  2. washthe solid residue is washed with additional methanol
  3. concentrationThe combined filtrate and washings are concentrated in vacuo
  4. customthe residue is partitioned between ethyl acetate and saturated aqueous ammonium chloride solution
  5. customThe organic phase is separated
  6. washwashed with saturated aqueous ammonium chloride solution, water and brine
  7. dry with materialdried over magnesium sulfate
  8. customRemoval of solvents in vacuo
  9. customgives an oil which
  10. customis chromatographed on a silica gel column (3:2 cyclohexane:ethyl acetate)

Sources & evidence

ORD record
ord-0e2d052dbfae41d586ef9b0f4efde441
Source dataset
uspto-grants-1983_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04378315

Reaction notes

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