HCID 13019676, compound → HCID 13019679, compound

HRID 2287191Notes

Reaction equation

HRID 2287191 reaction equation
Cl[CH2:2][C:3]([CH:5]1[O:11][CH:10]2[CH:7]([C:8](=[O:26])[N:9]2[C:12](=[C:23]([CH3:25])[CH3:24])[C:13]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:14])[N:6]1[C:27]([O:29][CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)=[O:28])=[O:4]>C(Cl)Cl.C(O)(=O)C.[Zn]>[C:3]([CH:5]1[O:11][CH:10]2[CH:7]([C:8](=[O:26])[N:9]2[C:12](=[C:23]([CH3:25])[CH3:24])[C:13]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:14])[N:6]1[C:27]([O:29][CH2:30][C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1)=[O:28])(=[O:4])[CH3:2]

Participants

5

Reactant 1

HCID 13019676HCID 13019676, compound

Product 1

HCID 13019679HCID 13019679, compoundYield 98%

Reagents, catalysts & solvents 3

HCID 23994ZincCatalystHCID 176Acetic AcidSolventHCID 6344DichloromethaneSolvent

Procedure

To a solution of 433 mg of benzyl α-(3ξ-chloroacetyl-2-carbobenzoxy-7-oxo-4-oxa-2,6-diazabicyclo[3.2.0]-heptan-6-yl)-α-isopropylideneacetate dissolved in a mixture of 4 ml of methylene chloride and 4 ml of acetic acid is added 450 mg of zinc powder, and the mixture stirred at room temperature for 1 hour. The reaction mixture is filtrated and the filtrate diluted with water and extracted with methylene chloride. The extract is washed with water, dried and evaporated to yield 375 mg of benzyl α-(3ξ-acetyl-2-carbobenzoxy-7-oxo-4-oxa-2,6-diazabicyclo[3.2.0]heptan-6-yl)-α-isopropylideneacetate as an oily material in 98% yield.

Workup

  1. filtrationThe reaction mixture is filtrated
  2. additionthe filtrate diluted with water
  3. extractionextracted with methylene chloride
  4. washThe extract is washed with water
  5. customdried
  6. customevaporated

Sources & evidence

ORD record
ord-1d7d32da4d2e44888d2e0433f2d776c7
Source dataset
uspto-grants-1981_05
Patent number
US04269773

Reaction notes

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