Dimethylformamide → HCID 16749113, compound

HRID 19927Notes

Reaction equation

HRID 19927 reaction equation
[Cl:1][C:2]1[C:3](O)=[C:4]([O:11][CH3:12])[CH:5]=[C:6]([CH:10]=1)C(O)=O.[CH2:14](Br)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[C:22](=[O:25])([O-])[O-:23].[K+].[K+].C(O[CH2:32][CH3:33])(=O)C.CN([CH:37]=[O:38])C>O>[CH2:14]([O:23][C:22](=[O:25])[C:6]1[CH:5]=[C:4]([O:11][CH3:12])[C:3]([O:38][CH2:37][C:33]2[CH:32]=[CH:6][CH:10]=[CH:2][CH:3]=2)=[C:2]([Cl:1])[CH:10]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

7

Procedure

A mixture of 5-chloro-vanillic acid (4.05 g, 20 mmol), benzyl bromide (8.55 g, 50 mmol) and potassium carbonate (6.90 g, 50 mmol) in DMF (60 mL) was stirred at room temperature for 18 hours. The mixture was transferred into a separation funnel and ethyl acetate (100 mL) and water (100 mL) were added, the organic layer was separated, washed with water (2×50 mL) and brine (50 mL), dried over sodium sulphate and concentrated under reduced pressure. The residue was crystallised from dichloromethane/hexane. Yield: 7.34 g (96%) colourless needles. 1H-NMR (400 MHz, CDCl3) δ 3.92 (s, 3H, —OCH3), 5.13 (s, 2H), 5.36 (s, 2H), 7.31-7.51 (m, 10H), 7.53 (d, J=2.0 Hz, 1H), 7.73 (d, J=2.0 Hz, 1H). LRMS (FAB+): 91.0 (100), 382.1 (15, [M+H]+).

Workup

  1. customThe mixture was transferred into a separation funnel
  2. customthe organic layer was separated
  3. washwashed with water (2×50 mL) and brine (50 mL)
  4. dry with materialdried over sodium sulphate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was crystallised from dichloromethane/hexane

Sources & evidence

ORD record
ord-fb19b0a28686499a9ed4301024e7e124
Source dataset
uspto-grants-2010_06
Patent number
US07745472B2

Reaction notes

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