4-Chlororesorcinol → HCID 86606719, compound

HRID 1393532Notes

Reaction equation

HRID 1393532 reaction equation
[Cl:1][C:2]1[CH:8]=[CH:7][C:5]([OH:6])=[CH:4][C:3]=1[OH:9].C(N(CC)CC)C.[C:17](Cl)(=[O:20])[CH:18]=[CH2:19].[CH2:22]1C[O:25][CH2:24][CH2:23]1>C(Cl)Cl>[C:17]([O:6][C:5]1[CH:7]=[CH:8][C:2]([Cl:1])=[C:3]([O:9][C:24](=[O:25])[CH:23]=[CH2:22])[CH:4]=1)(=[O:20])[CH:18]=[CH2:19]

Participants

6

Reactant 4

HCID 17314-ChlororesorcinolHCID 8028Tetrahydrofuran3×HCID 8471TriethylamineHCID 13140Acryloyl chloride

Product 1

HCID 86606719HCID 86606719, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 4-chlororesorcinol (86.76 g, 0.60 mol) in anhydrous THF (750 mL) in a 2-liter three neck round bottom flask equipped with dry nitrogen purge, thermocouple, condenser, and ice-water bath, triethylamine (163.6 g, 1.62 mol) in anhydrous THF (100 mL) was added dropwise in 10 minutes. After 10 minutes, acryloyl chloride (136 g, 1.5 mol) in anhydrous THF (300 mL) was added dropwise in 30-60 minutes (maintain 0-5 C of the solution). A precipitate formed immediately, and the mixture was warmed to room temperature and stirred overnight (˜15 hrs). The resulting mixture was filtered to remove the solid, and the filtrate was concentrated by rotary evaporation to give a darkly colored viscous liquid. The liquid was dissolved in methylene chloride (200 mL), cooled in an ice bath, washed with 1.0 N sodium hydroxide until pH>10, washed with 1.0 N HCl until pH<2, washed with DI water until pH>5, and dried over anhydrous sodium sulfate. The compound was purified by column chromatography and vacuum concentrated at room temperature to give a pale yellow or colorless liquid.

Workup

  1. custompurge
  2. temperaturemaintain 0-5 C of the solution)
  3. customA precipitate formed immediately
  4. filtrationThe resulting mixture was filtered
  5. customto remove the solid
  6. concentrationthe filtrate was concentrated by rotary evaporation
  7. customto give a darkly colored viscous liquid
  8. temperaturecooled in an ice bath
  9. washwashed with 1.0 N sodium hydroxide until pH>10
  10. washwashed with 1.0 N HCl until pH<2
  11. washwashed with DI water until pH>5
  12. dry with materialdried over anhydrous sodium sulfate
  13. customThe compound was purified by column chromatography and vacuum
  14. concentrationconcentrated at room temperature
  15. customto give a pale yellow or colorless liquid

Sources & evidence

ORD record
ord-3a735cb01cb54724aa4b8eae5958a906
Source dataset
uspto-grants-2008_03
Patent number
US07345134B2

Reaction notes

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