Pyridine → 1-(t-Butyldimethylsilyl)-4-(2-oxoethyl)-2-azetidinone

HRID 1493465Notes

Reaction equation

HRID 1493465 reaction equation
N1C=CC=CC=1.[Si:7]([N:14]1[CH:17]([CH2:18][CH2:19][OH:20])[CH2:16][C:15]1=[O:21])([C:10]([CH3:13])([CH3:12])[CH3:11])([CH3:9])[CH3:8]>C(Cl)Cl.[O-2].[O-2].[O-2].[Cr+6]>[Si:7]([N:14]1[CH:17]([CH2:18][CH:19]=[O:20])[CH2:16][C:15]1=[O:21])([C:10]([CH3:13])([CH3:12])[CH3:11])([CH3:9])[CH3:8]

Participants

5

Reactant 2

HCID 1049PyridineHCID 13104623N-(t-butyldimethylsilyl)-4-(2-hydroxyethyl)-azetidin-2-one

Product 1

HCID 128047181-(t-Butyldimethylsilyl)-4-(2-oxoethyl)-2-azetidinoneYield 73.5%

Reagents, catalysts & solvents 2

HCID 10219390chromium (VI) trioxideCatalystHCID 6344DichloromethaneSolvent2×

Procedure

Anhydrous chromium trioxide (CrO3) (1.94 g, 19.4 mmol) is added to a solution of anhydrous pyridine (3.07 g, 38.8 mmole) in anhydrous methylene chloride (CH2Cl2) (50 ml). The resulting mixture is stirred at room temperature for 15 mins. A solution of N-(t-butyldimethylsilyl)-4-(2-hydroxyethyl)-azetidin-2-one (0.74 g, 3.23 mmol) in anhydrous CH2Cl2 (5 ml) is added all at once. After stirring at room temperature for 5 mins, the mixture is decanted and the dark, gummy residue is washed with more CH2Cl2. The combined CH2Cl2 supernatant is evaporated i.v. The residue is taken up in diethyl ether and filtered to remove chromium salts. The ethereal filtrate is washed with 5% NaHCO3, 5% HCl, 5% NaHCO3 and brine, dried with MgSO4, filtered, and evaporated i.v. to yield N-(t-butyldimethylsilyl)-4-(2-oxoethyl)-azetidin-2-one (0.54 g) as an off-white solid: ir (CHCl3) 5.77, 5.80, 7.36, 7.60, 7.99, 8.50 and 11.95 cm-1 ; nmr (CDCl3) δ0.23 (s,3), 0.27 (s,3), 0.98 (s,9), 2.63 (ddd,1), 2.65 (dd,1), 3.07 (ddd,1), 3.37 (dd), 3.97 (m,1), and 9.78 (t,1); mass spectrum m/e 170 and 128.

Workup

  1. stirringAfter stirring at room temperature for 5 mins
  2. customthe mixture is decanted
  3. washthe dark, gummy residue is washed with more CH2Cl2
  4. customThe combined CH2Cl2 supernatant is evaporated i.v
  5. filtrationfiltered
  6. customto remove chromium salts
  7. washThe ethereal filtrate is washed with 5% NaHCO3, 5% HCl, 5% NaHCO3 and brine
  8. dry with materialdried with MgSO4
  9. filtrationfiltered
  10. customevaporated i.v

Sources & evidence

ORD record
ord-fd9bea1f02cb4e9d9d4898ec2df15843
Source dataset
uspto-grants-1991_06
Patent number
US05021566

Reaction notes

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