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Hydrochloric Acid → (S)-2-(1,4-Dibenzylpiperazin-2-yl)ethanol

HRID 131392
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HRID 131392 반응식
[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][C@@H:9]1[CH:21]=[CH2:22])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C12BC(CCC1)CCC2.[OH-:32].[Na+].OO.Cl>O.CC(OC)(C)C.CCCCCCC.C1COCC1>[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][C@@H:9]1[CH2:21][CH2:22][OH:32])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

10

반응물 5

HCID 313Hydrochloric AcidHCID 784Hydrogen PeroxideHCID 14798Sodium Hydroxide2회HCID 789669-Borabicyclo(3.3.1)nonaneHCID 17759473(S)-1,4-dibenzyl-2-vinylpiperazine

생성물 1

HCID 59732113(S)-2-(1,4-Dibenzylpiperazin-2-yl)ethanol수율 99.1%

시약·촉매·용매

4
HCID 962Water용매2회HCID 8028Tetrahydrofuran용매2회HCID 8900Heptane용매HCID 15413tert-Butyl methyl ether용매2회

실험 절차

Combine (S)-1,4-dibenzyl-2-vinyl-piperazine (131.0 g, 0.448 mol) and THF (500 mL) at ambient temperature. Add a 0.5M THF solution of 9-borabicyclo[3.3.1] nonane (9-BBN) (985.5 mL, 0.493 mol) over 20 minutes, keeping the pot temperature below 25° C. Stir the resulting mixture at ambient temperature for 16-18 hours. Cool the solution to 0-5° C. and quench with 3N NaOH (164.3 mL, 0.493 mol) over 5-10 minutes. Stir at 0-5° C. for 10-15 minutes and remove cooling bath. Add a 30% aqueous solution of hydrogen peroxide (160.2 mL, 1.57 mol) over 1 hour, maintaining a pot temperature of 30-35° C. Stir the resulting mixture for 1 hour and dilute with water (1.31 L) and MTBE (1.31 L). Layer separate and re-extract the aqueous layer with MTBE (655 mL). Combine organics and wash with water (2×655 mL) and brine (2×655 mL). Dry the MTBE solution over sodium sulfate, filter and concentrate in vacuo to afford 169.1 g of crude oil (theory=139.1 g). Treat the crude with 5N HCl (358 mL, 1.79 moles) and stir 5 minutes. Add water (250 mL) and stir 15-20 minutes. Add heptane (1.31 L) and stir 5 minutes. Layer separate and re-extract the aqueous layer with MTBE (655 mL). Discard these organic extracts and add 5N NaOH (403 mL, 2.02 moles) to the aqueous portion. Stir 5 minutes then dilute with MTBE (1.31 L) and layer separate. Re-extract the aqueous layer with MTBE (655 mL). Combine the MTBE extracts and wash with water (655 mL), then dry over sodium sulfate, filter and concentrate in vacuo to afford 137.8 g (99.0%) of the title compound. 1H NMR (500 MHz, DMSO-d6) δ 1.87 (m, 1H), 2.03 (m, 1H), 2.33 (m, 2H), 2.43 (m, 1H), 2.50 (d, 1H), 2.66 (d, 1H), 2.83 (m, 1H), 2.93 (m, 1H), 3.39 (d, 1H), 3.50 (m, 1H), 3.74 (m, 1H), 3.88 (m, 1H), 4.18 (d, 1H), 4.80 (bs, 1H), 7.26 (m,2H), 7.32 (m, 8H).

후처리

  1. customat ambient temperature
  2. customthe pot temperature below 25° C
  3. temperatureCool the solution to 0-5° C.
  4. stirringStir at 0-5° C. for 10-15 minutes
  5. customremove
  6. temperaturecooling bath
  7. temperaturemaintaining a pot temperature of 30-35° C
  8. stirringStir the resulting mixture for 1 hour
  9. customLayer separate
  10. extractionre-extract the aqueous layer with MTBE (655 mL)
  11. washCombine organics and wash with water (2×655 mL) and brine (2×655 mL)
  12. dry with materialDry the MTBE solution over sodium sulfate
  13. filtrationfilter
  14. concentrationconcentrate in vacuo
  15. customto afford 169.1 g of crude oil (theory=139.1 g)
  16. stirringstir 5 minutes
  17. customLayer separate
  18. extractionre-extract the aqueous layer with MTBE (655 mL)
  19. stirringStir 5 minutes
  20. customseparate
  21. washCombine the MTBE extracts and wash with water (655 mL)
  22. dry with materialdry over sodium sulfate
  23. filtrationfilter
  24. concentrationconcentrate in vacuo

출처 및 근거

ORD 기록
ord-ccbf88967ae942c5ae3a3f290cf2795d
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07384934B2

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