Isopropanol → 1-Phenoxy-4-[4-(4-fluorophenyl)-1-piperazinyl]-2-butanol

HRID 1639078Notes

Reaction equation

HRID 1639078 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.Cl[CH2:15][CH2:16][CH:17]([OH:26])[CH2:18][O:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C(=O)([O-])[O-].[Na+].[Na+].C(O)(C)C>C(O)CCC>[O:19]([CH2:18][CH:17]([OH:26])[CH2:16][CH2:15][N:11]1[CH2:12][CH2:13][N:8]([C:5]2[CH:4]=[CH:3][C:2]([F:1])=[CH:7][CH:6]=2)[CH2:9][CH2:10]1)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

Participants

6

Reactant 4

HCID 3776IsopropanolHCID 10340Sodium CarbonateHCID 752601-(4-Fluorophenyl)piperazineHCID 131203424-Chloro1-phenoxy-2-butanol

Product 1

HCID 144228391-Phenoxy-4-[4-(4-fluorophenyl)-1-piperazinyl]-2-butanol

Reagents, catalysts & solvents 1

HCID 2631-ButanolSolvent

Procedure

This compound was prepared according to the procedure of Example 6. A mixture of 3.6 g (0.02 mole) of 1-(4-fluorophenyl)piperazine, 4.0 g (0.02 mole) of 4-chloro-1-phenoxy 2-butanol and 5.3 g (0.05 mole) of anhydrous sodium carbonate in 100 ml of 1-butanol gave 5.1 g (74%) of offwhite powder, m.p. 97°-99° C. Recrystallizing solvent used was isopropyl alcohol.

Workup

  1. customThis compound was prepared
  2. customgave 5.1 g (74%) of offwhite powder, m.p. 97°-99° C

Sources & evidence

ORD record
ord-09bca7d0ca8340cba0f663eeb92cc099
Source dataset
uspto-grants-1989_11
Patent number
US04882330

Reaction notes

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