Sodium Hydroxide → HCID 86738265, compound

HRID 1902424Notes

Reaction equation

HRID 1902424 reaction equation
[CH3:1][N:2]1[C:8](=[O:9])[C:7]2[CH:10]=[CH:11][CH:12]=[CH:13][C:6]=2[NH:5][C:4](=[C:14](C(OCC)=O)[C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:3]1.[OH-].[Na+]>C(O)C>[CH3:1][N:2]1[C:8](=[O:9])[C:7]2[CH:10]=[CH:11][CH:12]=[CH:13][C:6]=2[NH:5][C:4](=[CH:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:3]1

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 20526886HCID 20526886, compound

Product 1

HCID 86738265HCID 86738265, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 33.2 g (0.1 mol) of diethyl (1,3,4,5-tetrahydro-4-methyl-5-oxo-2H-1,4-benzodiazepin-2-ylidene)malonate, 8.0 g (0.2 mol) of sodium hydroxide and 400 ml of absolute ethanol is heated to reflux for 3 hours. The mixture is subsequently left to crystallise at 0° C. and the separated solid material is filtered off under suction and transferred to a separating funnel. 100 ml of chloroform and 25 ml of water are added thereto. Then, the aqueous phase is separated. The organic phase is washed with 25 ml of water, dried over sodium sulphate and evaporated. There is obtained crystalline ethyl (1,3,4,5-tetrahydro-4-methyl-5-oxo-2H-1,4-benzodiazepin-2-ylidene)acetate of melting point 154°-155° C.

Workup

  1. temperatureis heated
  2. temperatureto reflux for 3 hours
  3. waitThe mixture is subsequently left
  4. customto crystallise at 0° C.
  5. filtrationthe separated solid material is filtered off under suction
  6. customtransferred to a separating funnel
  7. addition100 ml of chloroform and 25 ml of water are added
  8. customThen, the aqueous phase is separated
  9. washThe organic phase is washed with 25 ml of water
  10. dry with materialdried over sodium sulphate
  11. customevaporated

Sources & evidence

ORD record
ord-6b4ca408c29f4cb78f989519a3692c4e
Source dataset
uspto-grants-1982_12
Patent number
US04363762

Reaction notes

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