Acetic Acid → HCID 20298778, compound

HRID 1389313Notes

Reaction equation

HRID 1389313 reaction equation
Cl.Cl.[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10](=[O:31])[CH2:11][N:12]2[CH2:17][CH2:16][N:15]([CH:18]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:14][CH2:13]2)=[CH:6][C:5]=1[N+:32]([O-:34])=[O:33].CO.[BH4-].[Na+].C(O)(=O)C>O>[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([CH:10]([OH:31])[CH2:11][N:12]2[CH2:17][CH2:16][N:15]([CH:18]([C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)[C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[CH2:14][CH2:13]2)=[CH:6][C:5]=1[N+:32]([O-:34])=[O:33]

Participants

6

Procedure

To a stirred mixture of 5.2 parts of 1-(4-chloro-3-nitrophenyl)-2-[4-(diphenylmethyl)-1-piperazinyl]ethanone dihydrochloride in 40 parts of methanol are added portionwise 0.76 parts of sodium borohydride. Upon completion, stirring is continued for 30 minutes at room temperature. The reaction mixture is decomposed by the addition of a mixture of 2 parts of acetic acid and 10 parts of water. The solvent is evaporated and 50 parts of water are added to the residue. The whole is alkalized with ammonium hydroxide. The precipitated product is filtered off, washed with water and with a small amount of 2-propanol, and crystallized from ethanol, yielding 4.3 parts (95.1%) of α-(4-chloro-3-nitrophenyl)-4-(diphenylmethyl)-1-piperazineethanol; mp. 163.4° C.

Workup

  1. customThe solvent is evaporated
  2. addition50 parts of water are added to the residue
  3. filtrationThe precipitated product is filtered off
  4. washwashed with water and with a small amount of 2-propanol
  5. customcrystallized from ethanol

Sources & evidence

ORD record
ord-41d3c6e6d43f41c89a1f1d48c72a116e
Source dataset
uspto-grants-1981_01
Patent number
US04243806

Reaction notes

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