Ethyl 2,5-dimethyl-3-oxa-2,7-diazabicyclo[3.3.0]octane-7-carboxylate → 2,5-Dimethyl-3-oxa-2,7-diazabicyclo[3.3.0]octane

HRID 974912Notes

Reaction equation

HRID 974912 reaction equation
[CH3:1][N:2]1[O:9][CH2:8][C:7]2([CH3:10])[CH:3]1[CH2:4][N:5](C(OCC)=O)[CH2:6]2>O>[CH3:1][N:2]1[O:9][CH2:8][C:7]2([CH3:10])[CH:3]1[CH2:4][NH:5][CH2:6]2

Participants

3

Reactant 1

HCID 15070010Ethyl 2,5-dimethyl-3-oxa-2,7-diazabicyclo[3.3.0]octane-7-carboxylate

Product 1

HCID 150700112,5-Dimethyl-3-oxa-2,7-diazabicyclo[3.3.0]octane

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

13 g (60.6 mmol ) of ethyl 2,5-dimethyl-3-oxa-2,7-diazabicyclo[3.3.0]octane-7-carboxylate are heated under reflux with 33 g of Ba(OH)2 ·8H2O in 330 ml of water overnight. The BaCO3 is filtered off with suction, K2CO3 is added to the filtrate, the solid is filtered off with suction again and the filtrate is extracted ten times with 100 ml of CHCl3 each time. The extracts are dried over K2CO3 and concentrated and the residue is distilled.

Workup

  1. filtrationThe BaCO3 is filtered off with suction, K2CO3
  2. additionis added to the filtrate
  3. filtrationthe solid is filtered off with suction again
  4. extractionthe filtrate is extracted ten times with 100 ml of CHCl3 each time
  5. dry with materialThe extracts are dried over K2CO3
  6. concentrationconcentrated
  7. distillationthe residue is distilled

Sources & evidence

ORD record
ord-00eeb25e1dd14c9085ec3e3d565e167c
Source dataset
uspto-grants-1997_03
Patent number
US05607942

Reaction notes

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