Sulfuric Acid → 6-chloro-5-methoxy-2,3-dihydro-1H-inden-1-one

HRID 1788091Notes

Reaction equation

HRID 1788091 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH3:9].Cl[CH2:11][CH2:12][C:13](Cl)=[O:14].[Al+3].[Cl-].[Cl-].[Cl-].S(=O)(=O)(O)O>C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[C:6]2[C:5]([CH2:11][CH2:12][C:13]2=[O:14])=[CH:4][C:3]=1[O:8][CH3:9]

Participants

6

Conditions

Temperature
100 °C

Procedure

To a solution of 1-chloro-2-methoxybenzene (12.8 mL, 100 mmol) and 3-chloropropanoyl chloride (10.5 mL, 110 mmol) in CH2Cl2 (100 mL) at 0° C. was added AlCl3 (14.6 g, 110 mmol) portionwise during about 1 minute. After 30 minutes, sulfuric acid (300 mL) was poured slowly into the reaction mixture during about 3 minutes. The CH2Cl2 was removed by rotary evaporation under reduced pressure and the viscous residue was stirred at 100 ° C. for 2 hours. After cooling to ˜50° C., the viscous reaction mixture was poured cautiously onto 1.5 L of ice and allowed to stand overnight. The mixture was filtered and the cake of crude product was washed with water. The crude product was dissolved in 500 mL of 2% MeOH in CH2Cl2, dried over a mixture of Na2CO3 (˜10 g) and Na2SO4 (˜20 g), filtered and concentrated under vacuum to give 6-chloro-5-methoxyindan-1-one as an off-white solid.

Workup

  1. customThe CH2Cl2 was removed by rotary evaporation under reduced pressure
  2. temperatureAfter cooling to ˜50° C.
  3. additionthe viscous reaction mixture was poured cautiously onto 1.5 L of ice
  4. waitto stand overnight
  5. filtrationThe mixture was filtered
  6. washthe cake of crude product was washed with water
  7. dissolutionThe crude product was dissolved in 500 mL of 2% MeOH in CH2Cl2
  8. dry with materialdried over a mixture of Na2CO3 (˜10 g) and Na2SO4 (˜20 g)
  9. filtrationfiltered
  10. concentrationconcentrated under vacuum

Sources & evidence

ORD record
ord-9d32e44336ab474fa7ed89bdaf146243
Source dataset
uspto-grants-2009_03
Patent number
US07511152B2

Reaction notes

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