Hydrochloric Acid → HCID 178419208, compound

HRID 2244948Notes

Reaction equation

HRID 2244948 reaction equation
[Cl-].[Ce+3].[Cl-].[Cl-].[BH4-:5].[Na+].[C:7]([C:11]1[CH:12]=[C:13]([PH:23](=O)[C:24]2[CH:29]=[C:28]([C:30]([CH3:33])([CH3:32])[CH3:31])[C:27]([O:34][CH3:35])=[C:26]([C:36]([CH3:39])([CH3:38])[CH3:37])[CH:25]=2)[CH:14]=[C:15]([C:19]([CH3:22])([CH3:21])[CH3:20])[C:16]=1[O:17][CH3:18])([CH3:10])([CH3:9])[CH3:8].[H-].[Al+3].[Li+].[H-].[H-].[H-].Cl>C1COCC1.C1(C)C=CC=CC=1.O>[C:30]([C:28]1[CH:29]=[C:24]([PH:23][C:13]2[CH:12]=[C:11]([C:7]([CH3:10])([CH3:9])[CH3:8])[C:16]([O:17][CH3:18])=[C:15]([C:19]([CH3:22])([CH3:21])[CH3:20])[CH:14]=2)[CH:25]=[C:26]([C:36]([CH3:39])([CH3:38])[CH3:37])[C:27]=1[O:34][CH3:35])([CH3:31])([CH3:32])[CH3:33].[BH3:5]

Participants

9

Reactant 5

HCID 313Hydrochloric AcidHCID 24636Cerium(III) chlorideHCID 4311764Sodium borohydrideHCID 21226445Aluminium lithium hydrideHCID 178490127HCID 178490127, compound

Product 1

HCID 178419208HCID 178419208, compoundYield 39.6%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 1140TolueneSolventHCID 8028TetrahydrofuranSolvent

Procedure

Under an argon atmosphere, a solution of cerium chloride (4.55 g, 3.0 equivalents) in THF (25 mL) was stirred at room temperature (25° C.) for 30 min. Sodium borohydride (0.72 g, 3.1 equivalents) was added, and the mixture was stirred at room temperature for 1 hr. Then bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine oxide (3.0 g, 6.16 mmoL) synthesized in Reference Example 7 and lithium aluminum hydride (0.28 g, 1.2 equivalents) were successively added at 5° C., and the mixture was stirred at room temperature for 18 hrs. Water (10 mL) was added at 3° C., and toluene (30 mL) and 6M—HCl (20 mL) were added. The mixture was stirred at room temperature for 30 min. The reaction mixture was partitioned and the aqueous layer was extracted with toluene (30 mL). The combined organic layer was washed successively with 5% aqueous NaCl solution (20 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered by gravity, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (alumina 25 g, n-hexane). The residue was recrystallized from heptane to give the title compound (1.18 g, white crystals). yield 39.6%. melting point: 134.7° C. 1H-NMR (300 MHz, CDCl3, TMS) δ: 0.37-1.08 (m. 3H), 1.39 (s, 36H), 3.69 (s, 6H), 6.23 (dq, 1H, J=376.2 Hz, 6.78 Hz), 7.50 (d, 4H, J=12.18 Hz).

Workup

  1. additionwere successively added at 5° C.
  2. stirringthe mixture was stirred at room temperature for 18 hrs
  3. stirringThe mixture was stirred at room temperature for 30 min
  4. customThe reaction mixture was partitioned
  5. extractionthe aqueous layer was extracted with toluene (30 mL)
  6. washThe combined organic layer was washed successively with 5% aqueous NaCl solution (20 mL)
  7. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  8. filtrationfiltered by gravity
  9. concentrationthe filtrate was concentrated under reduced pressure
  10. customThe residue was purified by column chromatography (alumina 25 g, n-hexane)
  11. customThe residue was recrystallized from heptane

Sources & evidence

ORD record
ord-fd00bf8d45b34bea9c182b63545caeae
Source dataset
uspto-grants-2010_03
Patent number
US07678942B2

Reaction notes

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