Ammonium Chloride → 1-[5-(2-Bromophenyl)-1,5-dioxopentyl]pyrrolidine

HRID 1722343Notes

Reaction equation

HRID 1722343 reaction equation
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[Br:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13](=[O:21])[CH2:14][CH2:15][CH2:16][C:17](OC)=[O:18].[NH4+].[Cl-]>>[Br:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13](=[O:21])[CH2:14][CH2:15][CH2:16][C:17]([N:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1)=[O:18]

Participants

4

Reactant 3

HCID 25517Ammonium Chloride2×HCID 31268Pyrrolidine2×HCID 14582851Methyl 2-bromo-delta-oxobenzenepentanoate

Product 1

HCID 150876271-[5-(2-Bromophenyl)-1,5-dioxopentyl]pyrrolidine

Procedure

To 1ml of pyrrolidine is added with stirring 0.100g (0.35 mmol) of the product of Example 3, and 5mg of NH4Cl. The combined reagents were stirred in a sealed tube for 16 hours at room temperature. After this time, an additional 1ml of pyrrolidine and 5mg of NH4Cl was added and the reaction mixture was stirred an additional 16 hours. The solvent was removed under reduced pressure and the residue was flash chromatographed. Elution with diethyl ether produced 0.13g of the titled product, which was used without further purification.

Workup

  1. stirringthe reaction mixture was stirred an additional 16 hours
  2. customThe solvent was removed under reduced pressure
  3. customchromatographed
  4. washElution with diethyl ether

Sources & evidence

ORD record
ord-c07a163162294d7b9c2f9c20125ba723
Source dataset
uspto-grants-1989_08
Patent number
US04855324

Reaction notes

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