Di-tert-butyl dicarbonate → HCID 10331393, compound

HRID 520352Notes

Reaction equation

HRID 520352 reaction equation
[N:1]([C@H:4]1[C:8]([CH3:10])([CH3:9])[CH2:7][O:6][C:5]1=[O:11])=[N+]=[N-].[O:12](C(OC(C)(C)C)=O)[C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=O>CO.C(Cl)Cl.CCOC(C)=O.[Pd]>[CH3:9][C:8]1([CH3:10])[CH2:7][O:6][C:5](=[O:11])[C@H:4]1[NH:1][C:13](=[O:12])[O:15][C:16]([CH3:19])([CH3:18])[CH3:17]

Participants

7

Reactant 2

HCID 90495Di-tert-butyl dicarbonateHCID 10057735(S)-3-Azido-4,4-dimethyldihydrofuran-2(3H)-one

Product 1

HCID 10331393HCID 10331393, compound

Reagents, catalysts & solvents 4

HCID 23938PalladiumCatalystHCID 887MethanolSolventHCID 6344DichloromethaneSolventHCID 8857Ethyl AcetateSolvent

Procedure

To a solution of (S)-3-azido-4,4-dimethyldihydrofuran-2(3H)-one (5.52 g) in MeOH 910 mL) was added 10% Pd/C (0.379 g, 0.356 mmol) under N2. The reaction mixture was stirred under H2 at rt for 16 hrs. The reaction was filtered through diatomaceous earth (Celite®), washed with EtOAc and the filtrate was concentrated to yield a clear oil. To the above oil in DCM (10 mL) was added BOC2O (9.09 mL) and TEA (13.88 mL). The reaction mixture was stirred at rt for 16 hrs. The reaction mixture was diluted with EtOAc, washed with sat. NaHCO3, citric acid, water, sat. NaCl, dried over anhydrous Na2SO4, filtered and concentrated to yield an oil. The crude product was purified by silica gel chromatography (0-100% EtOAc in hexane) to yield (S)-tert-butyl 4,4-dimethyl-2-oxotetrahydrofuran-3-ylcarbamate (3.8 g) as a white solid. LC/MS (Cond. N-1): [M+Na]+ 252.06, RT=2.75 min. 1H NMR (400 MHz, CHLOROFORM-d) ppm 4.81-4.95 (1H, m), 4.38 (1H, d, J=7.78 Hz), 3.97-4.07 (2H, m), 1.47 (9H, s), 1.25 (3H, s), 1.01 (3H, s).

Workup

  1. filtrationThe reaction was filtered through diatomaceous earth (Celite®)
  2. washwashed with EtOAc
  3. concentrationthe filtrate was concentrated
  4. customto yield a clear oil
  5. stirringThe reaction mixture was stirred at rt for 16 hrs
  6. washwashed with sat. NaHCO3, citric acid, water, sat. NaCl
  7. dry with materialdried over anhydrous Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customto yield an oil
  11. customThe crude product was purified by silica gel chromatography (0-100% EtOAc in hexane)

Sources & evidence

ORD record
ord-2500128def064324a78f9ab3b52dfdd6
Source dataset
uspto-grants-2016_05
Patent number
US09326973B2

Reaction notes

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