Aluminium lithium hydride → 2-(2-Nonadecynyl)-1,3-propanediol

HRID 1885461Notes

Reaction equation

HRID 1885461 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[C:7]([CH:26]([C:32](OCC)=[O:33])[C:27](OCC)=[O:28])#[C:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]>CCOCC>[CH2:7]([CH:26]([CH2:27][OH:28])[CH2:32][OH:33])[C:8]#[C:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]

Participants

4

Procedure

A mixture of 1.8 g of lithium aluminum hydride in 150 ml of ether is prepared at 0° C. To this is added a solution of 11.7 g of 2-nonadecynylpropanedioic acid, diethyl ester in ether. This mixture is refluxed for 4 hours then the reaction is quenched with aqueous sodium sulfate. After stirring for 2 days, the reaction is diluted with ethyl acetate and filtered. The residue is treated with methanol, 1N sodium hydroxide and tetrahydrofuran and then evaporated. The residue is dissolved in ether and washed with brine and purified by flash chromatography, (4:6 ethyl acetate:petroleum ether), to give 5.3 g of the desired product as white plates, mp. 55° C.

Workup

  1. customis prepared at 0° C
  2. temperatureThis mixture is refluxed for 4 hours
  3. customthe reaction is quenched with aqueous sodium sulfate
  4. additionthe reaction is diluted with ethyl acetate
  5. filtrationfiltered
  6. additionThe residue is treated with methanol, 1N sodium hydroxide and tetrahydrofuran
  7. customevaporated
  8. dissolutionThe residue is dissolved in ether
  9. washwashed with brine
  10. custompurified by flash chromatography, (4:6 ethyl acetate:petroleum ether),

Sources & evidence

ORD record
ord-7ee34da4dd76460d80087f5f08feedb8
Source dataset
uspto-grants-1992_09
Patent number
US05144045

Reaction notes

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