Sodium Carbonate → HCID 86682894, compound

HRID 1522859Notes

Reaction equation

HRID 1522859 reaction equation
[NH2:1][C@@H:2]([CH3:5])[CH2:3][OH:4].Br[CH2:7][CH2:8][CH2:9][CH:10](Br)[CH3:11].C([O-])([O-])=O.[Na+].[Na+]>CCO>[CH3:7][C@H:8]1[CH2:9][CH2:10][CH2:11][N:1]1[C@@H:2]([CH3:5])[CH2:3][OH:4]

Participants

5

Conditions

Temperature
100 °C

Procedure

A mixture of (S)-2-aminopropan-1-ol (12.5 g, 0.166 mol), 1,4-dibromopentane (42 g, 0.18 mol) and Na2CO3 (53 g, 0.51 mol) in EtOH (800 mL) was heated at 100° C. for 24 h. The mixture was filtered, and the filter cake was washed with EtOH (50 mL). The combined filtrate was concentrated under reduced pressure, and the crude product was purified on a silica gel column (NH4OH/MeOH/DCM=1/6/300) to give (S)-2-((S)-2-methylpyrrolidin-1-yl)propan-1-ol (2.1 g) as a colorless oil and a crude mixture containing (S)-2-((R)-2-methylpyrrolidin-1-yl)propan-1-ol. 1H NMR (DMSO-d6): δ 4.22 (br s, 1H), 3.36 (dd, 1H), 3.22 (dd, 1H), 2.82 (m, 1H), 2.65 (m, 2H), 2.42 (q, 1H), 1.78 (m, 1H), 1.60 (m, 2H), 1.25 (m, 1H), 0.95 (d, 3H), 0.84 (d, 3H); LCMS: 144 (M+H)+.

Workup

  1. filtrationThe mixture was filtered
  2. washthe filter cake was washed with EtOH (50 mL)
  3. concentrationThe combined filtrate was concentrated under reduced pressure
  4. customthe crude product was purified on a silica gel column (NH4OH/MeOH/DCM=1/6/300)

Sources & evidence

ORD record
ord-aa3a19accb844159bbb104a060015152
Source dataset
uspto-grants-2015_07
Patent number
US09078871B2

Reaction notes

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