Ethanol → HCID 53766880, compound

HRID 1074327Notes

Reaction equation

HRID 1074327 reaction equation
[CH:1]([O:3][N:4]=[C:5]([C:11]1([O:16][CH2:15][CH2:14][O:13]1)[CH3:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH2:2].[CH:17]([Br:20])(Br)[Br:18].C(O)C.[OH-].[Na+]>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.C(Cl)Cl>[Br:18][C:17]1([Br:20])[CH2:2][CH:1]1[O:3][N:4]=[C:5]([C:11]1([O:13][CH2:14][CH2:15][O:16]1)[CH3:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7]

Participants

7

Procedure

To a solution of ethyl 2-vinyloxyimino-3,3-ethylenedioxybutyrate (syn isomer)(l5 g) and benzyltriethylammonium chloride (164 mg) in a mixture of methylene chloride (13 ml), bromoform (11.4 ml) and ethanol (0.65 ml) was added 50% aqueous solution of sodium hydroxide (105 ml) under ice-cooling. The mixture was stirred for 1 hour at the same temperature and allowed to be stirred at ambient temperature overnight. The mixture was extracted with diethyl ether. The extract was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was subjected to column chromatography on silica gel using a mixture of chloroform and ethyl acetate (4:1 V/V) as an eluent to give ethyl 2-(2,2-dibromocyclopropyloxyimino)-3,3-ethylenedioxybutyrate (syn isomer)(15.4 g) as an oil.

Workup

  1. temperaturecooling
  2. stirringto be stirred at ambient temperature overnight
  3. extractionThe mixture was extracted with diethyl ether
  4. washThe extract was washed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. additiona mixture of chloroform and ethyl acetate (4:1 V/V) as an eluent

Sources & evidence

ORD record
ord-0fc49886362241b5b3fda53342bc73bb
Source dataset
uspto-grants-1990_11
Patent number
US04973699

Reaction notes

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