Cyclohexanone → HCID 23312313, compound

HRID 2057424Notes

Reaction equation

HRID 2057424 reaction equation
C([Li])CCC.[CH3:6][N:7]1[CH2:12][CH2:11][CH:10]([C:13]2[O:14][C:15]3[CH:21]=[CH:20][C:19](Br)=[CH:18][C:16]=3[CH:17]=2)[CH2:9][CH2:8]1.[C:23]1(=[O:29])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1>C(OCC)C>[CH3:6][N:7]1[CH2:12][CH2:11][CH:10]([C:13]2[O:14][C:15]3[CH:21]=[CH:20][C:19]([C:23]4([OH:29])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]4)=[CH:18][C:16]=3[CH:17]=2)[CH2:9][CH2:8]1

Participants

5

Reactant 3

HCID 7967CyclohexanoneHCID 23312316HCID 23312316, compoundHCID 178418339Butyllithium

Product 1

HCID 23312313HCID 23312313, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent3×

Procedure

480 ml of a 1.35 N solution of n-butyl lithium in abs. diethyl ether is added dropwise within 30 minutes at -5° to a solution of 60 g of 1-methyl-4-(5-bromo-2-benzofuranyl)-piperidine [cp. Example 19] in 300 ml of diethyl ether. The reaction temperature during the dropwise addition is maintained at between -50° and 0° by external cooling. The solution is afterwards stirred for a further 90 minutes at 5° to 10°. There is then added dropwise within 30 minutes a solution of 85 ml of cyclohexanone in 100 ml of abs. diethyl ether, with the reaction temperature being kept at 0° to 5° by external cooling. The reaction solution is subsequently stirred for 15 hours at room temprature, and then poured, with stirring, onto 300 g of ice, and the aqueous phase extracted three times with 500 ml of ethyl acetate each time. The combined organic extracts are dried over sodium sulphate, filtered, and concentrated by evaporation. The residue is dissolved in 300 ml of 2 N hydrochloric acid, and the acid solution washed with ether. The aqueous solution is then adjusted by addition of 10% sodium hydroxide solution to pH 12, and extracted with 1000 ml of chloroform. The chloroform solution is dried with sodium sulphate, filtered off, and concentrated by evaporation to obtain crude 1-methyl-4-[5-(1-hydroxycyclohexyl)-2-benzofuranyl]-piperidine. The free base melts at 155° to 157° after recrystallisation from cyclohexane. The hydrochloride is prepared with hydrogen chloride in ethyl acetate, and recrystallised from acetone, whereupon it melts at 226°-229°.

Workup

  1. additionThe reaction temperature during the dropwise addition
  2. temperatureis maintained at between -50° and 0° by external cooling
  3. custombeing kept at 0° to 5° by external cooling
  4. stirringThe reaction solution is subsequently stirred for 15 hours at room temprature
  5. additionpoured
  6. extractionthe aqueous phase extracted three times with 500 ml of ethyl acetate each time
  7. dry with materialThe combined organic extracts are dried over sodium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated by evaporation
  10. dissolutionThe residue is dissolved in 300 ml of 2 N hydrochloric acid
  11. washthe acid solution washed with ether
  12. additionThe aqueous solution is then adjusted by addition of 10% sodium hydroxide solution to pH 12
  13. extractionextracted with 1000 ml of chloroform
  14. dry with materialThe chloroform solution is dried with sodium sulphate
  15. filtrationfiltered off
  16. concentrationconcentrated by evaporation

Sources & evidence

ORD record
ord-3ba66d033e434c9bb17643393b1f83ae
Source dataset
uspto-grants-1980_07
Patent number
US04210655

Reaction notes

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