Ethyl Acetate → HCID 14839581, compound

HRID 1031571Notes

Reaction equation

HRID 1031571 reaction equation
Cl[CH2:2][CH:3]1[CH2:8][N:7]([CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH2:6][CH2:5][N:4]1[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.[C:23]1(=[O:33])[NH:27][C:26](=[O:28])[C:25]2=[CH:29][CH:30]=[CH:31][CH:32]=[C:24]12.[K].C(OCC)(=O)C>CN(C)C=O.C(OC(C)C)(C)C>[C:23]1(=[O:33])[N:27]([CH2:2][CH:3]2[CH2:8][N:7]([CH2:9][C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH2:6][CH2:5][N:4]2[CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:26](=[O:28])[C:25]2=[CH:29][CH:30]=[CH:31][CH:32]=[C:24]12

Participants

6

Conditions

Temperature
110 °C

Procedure

A suspension of 15 g (47.6 mmol) of 2-chloromethyl-1,4-diphenylmethyl piperazine and 8.81 g (47.6 mmol) of potassium phtalimide in 7 ml anhydrous dimethyl formamide was stirred 2 hours at 110° C. After cooling the reaction mixture was taken up with 100 ml ethyl acetate. The mineral salts were filtered off. The solvent was removed, the residue was dissolved in 150 ml ethyl acetate, washed three times with water, dried over magnesium sulfate to give a srystalline product which was resrystallized in isopropyl ether to yield 6.67 g (33%) of title compound. M.P. 124° C.

Workup

  1. temperatureAfter cooling the reaction mixture
  2. filtrationThe mineral salts were filtered off
  3. customThe solvent was removed
  4. dissolutionthe residue was dissolved in 150 ml ethyl acetate
  5. washwashed three times with water
  6. dry with materialdried over magnesium sulfate
  7. customto give a srystalline product which

Sources & evidence

ORD record
ord-b52ba38270884ab89c2a2ecf0ea37fcb
Source dataset
uspto-grants-1990_09
Patent number
US04954507

Reaction notes

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