Water → 4-(2-Fluorophenyl)-1-methylpiperidin-4-OL

HRID 1248500노트

반응식

HRID 1248500 반응식
C([Li])CCC.Br[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[F:13].[CH3:14][N:15]1[CH2:20][CH2:19][C:18](=[O:21])[CH2:17][CH2:16]1.O>O1CCCC1>[F:13][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[C:18]1([OH:21])[CH2:19][CH2:20][N:15]([CH3:14])[CH2:16][CH2:17]1

참가 물질

6

반응물 4

HCID 962WaterHCID 612591-Bromo-2-fluorobenzeneHCID 740491-Methyl-4-piperidoneHCID 178418339Butyllithium

생성물 1

HCID 126940234-(2-Fluorophenyl)-1-methylpiperidin-4-OL

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

46 ml of 2.4M n-butyllithium are added over a 15 minute span to a mixture cooled to -70° C. of 17.5 g of 2-bromofluorobenzene and 50 ml of tetrahydrofuran. After total addition, the reaction mixture is stirred at between -60° to -70° C. for 15 minutes to enable complete lithiation, which results in a tan colored solution. A mixture of 11.3 g of 1-methyl-4-piperidone in 20 ml of tetrahydrofuran is added to the solution at a rate to maintain the reaction medium's temperature below -60° C. After total addition, the reaction mixture is stirred at the same low temperature for one hour before being permitted to warm to ambient temperature. Water is added and the biphasic mixture is permitted to separate into its organic and aqueous phases. The organic phase is collected and the aqueous phase is extracted thrice with ether and the ether extracts are combined with the organic phase. The combined organic solution is extracted with an excess of 2N hydrochloric acid and then discarded. The acidic solution is basified with ammonium hydroxide, producing a heavy oil which is dissolved in a 1:1 ethyl acetate ether mixture. This solution is dried and then concentrated to dryness, leaving a viscous oil which crystallizes with cooling. The solid product is recrystallized from a benzene-hexane mixture to give prisms, mp 127°-129° C. of 4-(2-fluorophenyl)-4-hydroxy-1-methylpiperidine.

후처리

  1. additionAfter total addition
  2. customresults in a tan colored solution
  3. additionis added to the solution at a rate
  4. temperatureto maintain the reaction medium's temperature below -60° C
  5. additionAfter total addition
  6. stirringthe reaction mixture is stirred at the same low temperature for one hour
  7. customto separate into its organic
  8. customThe organic phase is collected
  9. extractionthe aqueous phase is extracted thrice with ether
  10. extractionThe combined organic solution is extracted with an excess of 2N hydrochloric acid
  11. customproducing a heavy oil which
  12. customThis solution is dried
  13. concentrationconcentrated to dryness
  14. customleaving a viscous oil which
  15. customcrystallizes
  16. temperaturewith cooling
  17. customThe solid product is recrystallized from a benzene-hexane mixture

출처 및 근거

ORD 기록
ord-acbf289fdfc14376926f63965bf3996e
출처 데이터셋
uspto-grants-1985_06
특허 번호
US04524207

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