Boron trifluoride etherate → 850991-77-4

HRID 597991Notes

Reaction equation

HRID 597991 reaction equation
O[CH2:2][N:3]([CH2:9][CH:10]1[CH2:15][CH2:14][CH:13]=[CH:12][CH2:11]1)[C:4](=[O:8])[O:5][CH2:6][CH3:7].B(F)(F)F.CCOCC>ClCCl>[CH:10]12[CH2:15][CH:14]([CH:13]=[CH:12][CH2:11]1)[CH2:2][N:3]([C:4]([O:5][CH2:6][CH3:7])=[O:8])[CH2:9]2

Participants

4

Procedure

To a stirred solution of ethyl N-(hydroxymethyl)cyclohex-3-en-1-ylmethylcarbamate (213 mg, 1.00 mmol) in 15 mL of dichloromethane, cooled in an ice bath, was added drop-wise boron trifluoride etherate (0.19 mL, 1.5 mmol). The initially cloudy reaction mixture slowly cleared. After it had become homogenous, it was warmed to ambient temperature and stirred for 1.5 h. The reaction was quenched by sequential addition of 5 mL of water and 5 mL of 10% KOH solution. The mixture was extracted with dichloromethane (2×20 mL), and the combined extracts were washed with brine (25 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was column chromatographed on silica gel with 2:1 hexane/ethyl acetate to give the product as a colorless oil (145 mg, 74%).

Workup

  1. customThe initially cloudy reaction mixture
  2. customThe reaction was quenched by sequential addition of 5 mL of water and 5 mL of 10% KOH solution
  3. extractionThe mixture was extracted with dichloromethane (2×20 mL)
  4. washthe combined extracts were washed with brine (25 mL)
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customchromatographed on silica gel with 2:1 hexane/ethyl acetate

Sources & evidence

ORD record
ord-0b0c81ea4fbe424cbd1005a378c5e6e5
Source dataset
uspto-grants-2011_03
Patent number
US07897611B2

Reaction notes

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