Ethylene Glycol → HCID 13689820, compound

HRID 1388875Notes

Reaction equation

HRID 1388875 reaction equation
[CH2:1]([O:3][C:4]([C:6]1([C:25]([O:27][CH2:28][CH3:29])=[O:26])[CH:9]([C:10](=[O:12])[CH3:11])[C:8](=[O:13])[N:7]1[CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:16]=1[O:23][CH3:24])=[O:5])[CH3:2].[CH2:30](O)[CH2:31][OH:32].O.ClCCl>O1CCOCC1>[CH2:1]([O:3][C:4]([C:6]1([C:25]([O:27][CH2:28][CH3:29])=[O:26])[CH:9]([C:10]2([CH3:11])[O:32][CH2:31][CH2:30][O:12]2)[C:8](=[O:13])[N:7]1[CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:16]=1[O:23][CH3:24])=[O:5])[CH3:2]

Participants

6

Procedure

25.5 g (0.063 moles) of diethyl-3-acetyl-1-(2,4-dimethoxybenzyl)4-oxo-2,2-azetidine-dicarboxylate prepared according to Example (1e), 6.8 ml (0.126 moles, 7.8 g) of ethylene glycol and 15.8 ml (0.126 moles, 17.9 g) of borotrifluoride diethyl etherate in 100 ml of dry dioxane are allowed to stand at room temperature for 3 days, whereupon 150 ml of water and 150 ml of dichloromethane are added to the reaction mixture. Thereafter the organic phase is separated and shaken with 50 ml of a 5% aqueous sodium hydrogen-carbonate solution and 50 ml of water. The organic phase is separated again, dried with magnesium sulfate, filtered and the filtrate is evaporated. 23.6 g (84% of diethyl-1-(2.4-dimethoxybenzyl)-3-(2-methyl-1,3-dioxolan-2-yl)-4-oxo-2,2-azetidine-dicarboxylate are obtained.

Workup

  1. additionare added to the reaction mixture
  2. customThereafter the organic phase is separated
  3. customThe organic phase is separated again
  4. dry with materialdried with magnesium sulfate
  5. filtrationfiltered
  6. customthe filtrate is evaporated

Sources & evidence

ORD record
ord-6b51021b218f4dff957c594abce40934
Source dataset
uspto-grants-1984_02
Patent number
US04434099

Reaction notes

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