Water → HCID 612239, compound

HRID 1875367Notes

Reaction equation

HRID 1875367 reaction equation
[CH3:1][C:2]1[O:17][C:7]2[CH:8]=[C:9]3[O:16][CH:15]=[CH:14][C:10]3=[C:11]([O:12]C)[C:6]=2[C:4](=[O:5])[CH:3]=1.B(Cl)(Cl)Cl.O>ClCCl>[OH:12][C:11]1[C:10]2[CH:14]=[CH:15][O:16][C:9]=2[CH:8]=[C:7]2[C:6]=1[C:4](=[O:5])[CH:3]=[C:2]([CH3:1])[O:17]2

Participants

5

Conditions

Temperature
-78 °C

Procedure

To a suspension of visnagin (920 mg, 4.0 mmol) in dichloromethane (20 mL) at −78° C. was added a solution of boron trichloride (1.0 M, 4.0 mL, 4.0 mmol) and the reaction mixture was stirred at −78° C. for 15 min then rt for 16 h. The reaction mixture was cooled to 0° C. and water (25 mL) was added slowly at first. The organics were concentrated in vacuo and the resulting suspension was diluted with 5% citric acid (150 mL) and heated at 60° C. for 1 h. The suspension was filtered, washing with water (3×50 mL) and the resulting solid was dried in a vacuum oven to afford the title compound as a yellow solid (710 mg, 83%): 1H NMR (300 MHz, CDCl3): δ 2.38 (s, 3H), 6.06 (s, 1H), 6.97 (d, J=2.2 Hz, 1H), 6.99 (s, 1H), 7.55 (d, J=2.2 Hz, 1H), 13.52 (s, 1H). MS (ES+) m/z 217.2 (M+H+).

Workup

  1. waitrt for 16 h
  2. temperatureThe reaction mixture was cooled to 0° C.
  3. concentrationThe organics were concentrated in vacuo
  4. additionthe resulting suspension was diluted with 5% citric acid (150 mL)
  5. temperatureheated at 60° C. for 1 h
  6. filtrationThe suspension was filtered
  7. washwashing with water (3×50 mL)
  8. customthe resulting solid was dried in a vacuum oven

Sources & evidence

ORD record
ord-5430ef8b6cf74da1a208f233ce3f4505
Source dataset
uspto-grants-2012_11
Patent number
US08309545B2

Reaction notes

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