Hydrochloric Acid → HCID 21481314, compound

HRID 1283869Notes

Reaction equation

HRID 1283869 reaction equation
[CH3:1][C:2]1[C:13]([CH3:14])=[CH:12][CH:11]=[CH:10][C:3]=1[O:4][CH2:5][C:6]([O:8]C)=[O:7].[CH2:15]([CH:17]([C:21](Cl)=[O:22])[C:18](Cl)=[O:19])[CH3:16].[Cl-].[Al+3].[Cl-].[Cl-].Cl.[OH-].[K+]>C(Cl)Cl.CO>[O:19]=[C:18]1[C:11]2[C:12](=[C:13]([CH3:14])[C:2]([CH3:1])=[C:3]([O:4][CH2:5][C:6]([OH:8])=[O:7])[CH:10]=2)[C:21](=[O:22])[CH:17]1[CH2:15][CH3:16]

Participants

8

Conditions

Temperature
25 °C

Procedure

A solution of methyl (2,3-dimethylphenoxy)acetate (3.0 g., 0.0155 mole) and 2-ethylmalonyl chloride (2.7 g., 0.016 mole) in methylene chloride (200 ml.) is cooled to 0°C. then treated with aluminum chloride (6.6 g., 0.05 mole) in several portions during a 15 minute period. The reaction is stirred for 2 hours at 0°C., 18 hours at 25°C. then at reflux for six hours, cooled and poured into cold 1 N-hydrochloric acid (500 ml.), the organic layer is washed with water, saturated aqueous sodium chloride, dried over magnesium sulfate, then the solvent evaporated at reduced pressure. The crude methyl ester is hydrolyzed by treatment with potassium hydroxide (0.34 g., 0.005 mole) and methanol (20 ml.) at reflux for 1/2 hour, cooled and acidified with aqueous hydrochloric acid affording (1,3-dioxo-2-ethyl-4,5-dimethyl-6-indanyloxy)acetic acid which melts at 187°-193°C. after recrystallization from acetic acid-water.

Workup

  1. temperatureat reflux for six hours
  2. temperaturecooled
  3. washthe organic layer is washed with water, saturated aqueous sodium chloride
  4. dry with materialdried over magnesium sulfate
  5. customthe solvent evaporated at reduced pressure
  6. temperatureat reflux for 1/2 hour
  7. temperaturecooled

Sources & evidence

ORD record
ord-98281e259be440f894e13f9576887936
Source dataset
uspto-grants-1976_08
Patent number
US03976681

Reaction notes

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