Sodium Hydroxide → 1-[2-Fluoro-2-(4-nitrophenyl)ethyl]-4-[2-(4-nitrophenyl)ethyl]piperazine

HRID 1187131Notes

Reaction equation

HRID 1187131 reaction equation
CCN(S(F)(F)[F:7])CC.[N+:10]([C:13]1[CH:18]=[CH:17][C:16]([CH:19](O)[CH2:20][N:21]2[CH2:26][CH2:25][N:24]([CH2:27][CH2:28][C:29]3[CH:34]=[CH:33][C:32]([N+:35]([O-:37])=[O:36])=[CH:31][CH:30]=3)[CH2:23][CH2:22]2)=[CH:15][CH:14]=1)([O-:12])=[O:11].[OH-].[Na+]>C(Cl)Cl>[F:7][CH:19]([C:16]1[CH:15]=[CH:14][C:13]([N+:10]([O-:12])=[O:11])=[CH:18][CH:17]=1)[CH2:20][N:21]1[CH2:26][CH2:25][N:24]([CH2:27][CH2:28][C:29]2[CH:30]=[CH:31][C:32]([N+:35]([O-:37])=[O:36])=[CH:33][CH:34]=2)[CH2:23][CH2:22]1

Participants

5

Procedure

DAST (6.6 μL, 0.050 mmol) was added to 1-(4-nitrophenyl)-2-{4-[2-(4-nitrophenyl)ethyl]piperazin-1-yl}ethanol (10 mg, 0.025 mmol) in DCM (1 mL) and the resulting mixture was stirred at RT for 72 h. Then 1 N NaOH was added and the mixture was extracted twice with DCM. The combined organic layers were dried over MgSO4, filtered, and evaporated to dryness. The crude product was purified by mass directed preparative HPLC to yield 1-[2-fluoro-2-(4-nitrophenyl)ethyl]-4-[2-(4-nitrophenyl)ethyl]piperazine.

Workup

  1. extractionthe mixture was extracted twice with DCM
  2. dry with materialThe combined organic layers were dried over MgSO4
  3. filtrationfiltered
  4. customevaporated to dryness
  5. customThe crude product was purified by mass

Sources & evidence

ORD record
ord-7000dc532c014466bf2112bdf02bbfdb
Source dataset
uspto-grants-2014_03
Patent number
US08673920B2

Reaction notes

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