Tetrahydrofuran → HCID 18918573, compound

HRID 1290551Notes

Reaction equation

HRID 1290551 reaction equation
[CH3:1][N:2]([CH3:16])[C:3]1[CH:8]=[CH:7][N:6]=[CH:5][C:4]=1[CH:9]([CH3:15])C(OCC)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].[O:23]1CCC[CH2:24]1>>[CH3:16][N:2]([CH3:1])[C:3]1[CH:8]=[CH:7][N:6]=[CH:5][C:4]=1[CH2:9][CH2:15][CH2:24][OH:23]

Participants

4

Reactant 3

HCID 8028TetrahydrofuranHCID 18918255HCID 18918255, compoundHCID 21226445Aluminium lithium hydride

Product 1

HCID 18918573HCID 18918573, compound

Procedure

To a stirred solution of the product of step iv) (2.6 g) in tetrahydrofuran (100 ml) was added lithium aluminium hydride (1.2 g) and the resulting suspension stirred for 4 hours at ambient temperature. Excess reducing agent was destroyed by the sequential addition of ethyl acetate, water, and conc. HCl. The mixture was then basified and extracted sequentially with ethyl acetate and dichloromethane. The organic extracts were combined, dried (PS paper and MgSO4) and evaporated to yield 4-dimethylamino-3-(3-hydroxypropyl)pyridine as a pale yellow oil (2.2 g), essentially pure by Tlc; NMR (d6DMSO) δ 1.6-1.8(2H,m): 2.65(2H,t); 2.8(6H,s); 3.5(2H,t); 4.5(1H,brs); 6.7(2H,d); 8.2(2H,d); m/e 181 (M+H)+.

Workup

  1. customwas destroyed by the sequential addition of ethyl acetate, water, and conc. HCl
  2. extractionextracted sequentially with ethyl acetate and dichloromethane
  3. dry with materialdried (PS paper and MgSO4)
  4. customevaporated

Sources & evidence

ORD record
ord-ffbf13b78eef44dfa62ffcc31493061a
Source dataset
uspto-grants-1998_05
Patent number
US05750754

Reaction notes

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