Benzene → HCID 131710372, compound

HRID 2071207Notes

Reaction equation

HRID 2071207 reaction equation
[CH2:1]([C:3]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH3:14])[C:4]=1[NH:5][CH2:6][CH:7]=[O:8])[CH3:2].C(=O)([O-])[O-].[Na+].[Na+].C1C=CC=CC=1.[Cl:27][C:28](=[O:33])[CH:29](Cl)[CH2:30][CH3:31]>O>[Cl:27][C:28](=[O:33])[CH:29]([N:5]([CH2:6][CH:7]=[O:8])[C:4]1[C:9]([O:13][CH3:14])=[CH:10][CH:11]=[CH:12][C:3]=1[CH2:1][CH3:2])[CH2:30][CH3:31]

Participants

6

Reactant 4

HCID 241BenzeneHCID 10340Sodium CarbonateHCID 1390532-Chlorobutanoyl chlorideHCID 21412824HCID 21412824, compound

Product 1

HCID 131710372HCID 131710372, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

The dimethyl acetal of 2-(2-ethyl-6-methoxyanilino)-acetaldehyde (0.1 mole), sodium carbonate (0.06 mole) dissolved in water (50 ml) and benzene (50 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and cooling means. The mixture is cooled to a temperature of about 0° C. and α-chlorobutanoyl chloride (0.11 mole) is incrementally added with stirring. After the addition is completed stirring is continued and the reaction mixture is permitted to warm to room temperature. After this time the mixture is filtered, washed with dilute hydrochloric acid and stripped of solvent to yield the desired product the dimethyl acetal of 2-(N-α-chlorobutanoyl-2-ethyl-6-methoxyanilino)acetaldehyde.

Workup

  1. customequipped with a mechanical stirrer
  2. temperaturethermometer and cooling means
  3. additionis incrementally added
  4. additionAfter the addition
  5. stirringis completed stirring
  6. filtrationAfter this time the mixture is filtered
  7. washwashed with dilute hydrochloric acid

Sources & evidence

ORD record
ord-4e53dacebe06482683a44c61305114a6
Source dataset
uspto-grants-1977_09
Patent number
US04046554

Reaction notes

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