Dodecanoyl chloride → HCID 15037163, compound

HRID 488246Notes

Reaction equation

HRID 488246 reaction equation
[CH3:1][C:2]1[O:6][C:5]([Si:7]([CH2:12][CH3:13])([CH2:10][CH3:11])[CH2:8][CH3:9])=[CH:4][C:3]=1[CH2:14][OH:15].C(N(CC)CC)C.[C:23](Cl)(=[O:35])[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34]>O1CCCC1>[C:23]([O:15][CH2:14][C:3]1[CH:4]=[C:5]([Si:7]([CH2:12][CH3:13])([CH2:10][CH3:11])[CH2:8][CH3:9])[O:6][C:2]=1[CH3:1])(=[O:35])[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34]

Participants

5

Reactant 3

HCID 8166Dodecanoyl chlorideHCID 8471TriethylamineHCID 15037162HCID 15037162, compound

Product 1

HCID 15037163HCID 15037163, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a stirred solution of 5-methyl-2-triethylsilyl-4-furylmethanol (208 mg. 0.92 mmol) and triethylamine (121 mg, 1.20 mmol) in tetrahydrofuran (10 ml) at 0 degrees under argon was added lauroyl chloride 302 mg, 1.38 mmol). This solution was allowed to warm gradually to room temperature and quenched with a 10% aqueous HCl solution. The organics were extracted into hexanes and the combined fractions were washed with a saturated aqueous solution of sodium bicarbonate, H2O and brine Evaporation of the dried (magnesium sulfate) extracts gave an oil which was purified by filtration through silica using 2% ethyl ether/hexanes to give the title compound.

Workup

  1. customquenched with a 10% aqueous HCl solution
  2. extractionThe organics were extracted into hexanes
  3. washthe combined fractions were washed with a saturated aqueous solution of sodium bicarbonate, H2O and brine Evaporation of the
  4. dry with materialdried (magnesium sulfate)
  5. customextracts gave an oil which
  6. filtrationwas purified by filtration through silica using 2% ethyl ether/hexanes

Sources & evidence

ORD record
ord-3539fcdb188e410d8cb7f568d0e41268
Source dataset
uspto-grants-1994_03
Patent number
US05298633

Reaction notes

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