Pyrrolidine → HCID 58764212, compound

HRID 2387086Notes

Reaction equation

HRID 2387086 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8]Br)=[C:4]([CH2:10][CH3:11])[CH:3]=1.[NH:12]1[CH2:16][CH2:15][CH2:14][CH2:13]1>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)=[C:4]([CH2:10][CH3:11])[CH:3]=1

Participants

4

Reactant 2

HCID 31268PyrrolidineHCID 587640754-Bromo-1-(bromomethyl)-2-ethylbenzene

Product 1

HCID 58764212HCID 58764212, compoundYield 68%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 4-bromo-1-bromomethyl-2-ethyl-benzene (2.00 g, 7.19 mmol) in CH2Cl2 (30 mL) was added dropwise pyrrolidine (1.19 mL, 14.4 mmol). The mixture was stirred for 15 hours, and then partitioned between Et2O and H2O. The organic layer was washed with brine, dried over MgSO4, and concentrated to yield a yellow oil (1.3 g, 68%). 1H NMR (300 MHz, CDCl3): δ 1.19 (t, J=7.5 Hz, 3 H), 1.76 (m, 4 H), 2.47 (m, 4 H), 2.69 (q, J=7.5 Hz, 2 H), 3.54 (s, 2 H), 7.19 (m, 1 H), 7.25 (m, 1 H), 7.29 (d, J=1.9 Hz, 1 H).

Workup

  1. custompartitioned between Et2O and H2O
  2. washThe organic layer was washed with brine
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-326f4c0683a84260af0b7605da0f3df1
Source dataset
uspto-grants-2012_09
Patent number
US08268835B2

Reaction notes

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