Ammonium Chloride → HCID 86615477, compound

HRID 2079580Notes

Reaction equation

HRID 2079580 reaction equation
[CH2:1]([O:3][P:4]([C:9]([C:17]#[N:18])=[CH:10][CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1)(=[O:8])[O:5][CH2:6][CH3:7])[CH3:2].[CH2:19]([Mg]Br)[CH:20]=[CH2:21].[Cl-].[NH4+]>C1COCC1>[CH2:6]([O:5][P:4]([CH:9]([C:17]#[N:18])[CH:10]([CH:11]1[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16]1)[CH2:21][CH:20]=[CH2:19])(=[O:8])[O:3][CH2:1][CH3:2])[CH3:7]

Participants

5

Conditions

Temperature
7.5 °C

Procedure

To a stirred mixture of the oil isolated in Step A (17.5 g, 65 mmol), and cuprous iodide (0.75 g) in THF (100 mL) at 0° C., a solution of allylmagnesium bromide in THF (2 M, 42 mL, 84 mmol) was added slowly while the temperature was maintained at about 5-10° C. The reaction mixture then was stirred at room temperature overnight. Aqueous saturated ammonium chloride solution (100 mL) was then added. The reaction mixture was stirred 30 min at room temperature and then extracted with ethyl acetate (200 mL). The organic solution washed with saturated ammonium chloride solution three times and with brine one time, and then was dried over sodium sulfate. The reaction mixture was then filtered and concentrated to yield a residue. The residue was purified by Kugelrohr distillation to yield a colorless oil (GC showed it contained 20% starting material, but the oil was used as is without further purification).

Workup

  1. stirringThe reaction mixture was stirred 30 min at room temperature
  2. extractionextracted with ethyl acetate (200 mL)
  3. washThe organic solution washed with saturated ammonium chloride solution three times and with brine one time
  4. dry with materialwas dried over sodium sulfate
  5. filtrationThe reaction mixture was then filtered
  6. concentrationconcentrated
  7. customto yield a residue
  8. distillationThe residue was purified by Kugelrohr distillation
  9. customto yield a colorless oil (GC
  10. customas is without further purification)

Sources & evidence

ORD record
ord-f9169a4d2bab45fb9106276aba784721
Source dataset
uspto-grants-2011_04
Patent number
US07932261B2

Reaction notes

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