Ammonium Chloride → HCID 178444289, compound

HRID 1530176Notes

Reaction equation

HRID 1530176 reaction equation
[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H:9]([CH:12]2[CH2:17][CH2:16][CH:15]([CH:18]3[CH2:23][CH2:22][C:21](=[O:24])[CH:20]=[CH:19]3)[CH2:14][CH2:13]2)[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5].[Cl-].[NH4+]>C1COCC1>[CH2:1]([C@H:6]1[CH2:7][CH2:8][C@H:9]([CH:12]2[CH2:17][CH2:16][CH:15]([CH:18]3[CH2:23][CH2:22][C:21]([CH2:6][CH2:1][CH2:2][CH3:3])([OH:24])[CH:20]=[CH:19]3)[CH2:14][CH2:13]2)[CH2:10][CH2:11]1)[CH2:2][CH2:3][CH2:4][CH3:5]

Participants

4

Reactant 2

HCID 25517Ammonium ChlorideHCID 178444288HCID 178444288, compound

Product 1

HCID 178444289HCID 178444289, compoundYield 199.9%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Under a nitrogen atmosphere, 4.0 g of 4-(4-(trans-4-pentylcyclohexyl)cyclohexyl)-2-cyclohexenone (r-9) was dissolved into 50 mL of THF, 14.5 mL of butylmagnesium bromide THF solution (1 M/L) was added dropwise thereto at room temperature, and the resultant mixture was stirred at 50° C. for 30 minutes, and then stirred at room temperature overnight. A saturated aqueous solution of ammonium chloride was added dropwise under ice-cooling, the resultant mixture was subjected to extraction with ethyl acetate, and then organic layers were combined, the resultant organic layer was washed with saturated brine, and then dried over anhydrous magnesium sulfate. A solvent was evaporated under reduced pressure, and the resultant residue was purified by fractionation on silica gel column chromatography (eluate:heptane:ethyl acetate=7:3 (in a volume ratio)), and thus 4.70 g of 4-(4-(trans-4-pentylcyclohexyl)cyclohexyl)-1-butyl-2-cyclohexene-1-ol (compound (r-10)) was obtained.

Workup

  1. additionwas added dropwise
  2. temperaturecooling
  3. extractionthe resultant mixture was subjected to extraction with ethyl acetate
  4. washthe resultant organic layer was washed with saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customA solvent was evaporated under reduced pressure
  7. customthe resultant residue was purified by fractionation on silica gel column chromatography (eluate:heptane

Sources & evidence

ORD record
ord-491872625f784f908dd7338548592da6
Source dataset
uspto-grants-2015_07
Patent number
US09090825B2

Reaction notes

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