Sodium hydride → O-(2-methoxybenzyl)-6-dimethylaminohexanol

HRID 272798

Reaktionsgleichung

Reaktionsgleichung von HRID 272798
[CH3:1][N:2]([CH3:10])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][OH:9].[H-].[Na+].[CH3:13][O:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17]Cl>C1COCC1.CN(C=O)C>[CH3:13][O:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17][O:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][N:2]([CH3:10])[CH3:1]

Komponenten

5

Versuchsvorschrift

6-Dimethylamino-1-hexanol (8.80 g, 60.6 mmol) was dissolved in 2/1 mixture of THF/DMF (150 mL) and the solution was cooled in an ice/water bath. Sodium hydride (3.25 g, 80.8 mmol, 60% in oil) was added. After 40 min., 2-methoxybenzyl chloride (6.28 g, 40.4 mmol) was added and the solution was allowed to warm to room temperature over 1 h. After 3 h, the reaction was quenched by the addition of 1M NaHSO4. Tetrahydrofuran was removed in vacuo, and the solution was washed with EtOAc. The aqueous phase was basified with 3M NaOH and extracted with ether. The combined ether phases were dried over K2CO3, filtered, and the product was crystallized by the addition of 4M HCl/dioxane to give O-(2-methoxybenzyl)-6-dimethylaminohexanol (10.4 g) as a white solid.

Aufarbeitung

  1. temperaturethe solution was cooled in an ice/water bath
  2. waitAfter 3 h
  3. customthe reaction was quenched by the addition of 1M NaHSO4
  4. customTetrahydrofuran was removed in vacuo
  5. washthe solution was washed with EtOAc
  6. extractionextracted with ether
  7. dry with materialThe combined ether phases were dried over K2CO3
  8. filtrationfiltered
  9. customthe product was crystallized by the addition of 4M HCl/dioxane

Quellen und Nachweise

ORD-Eintrag
ord-ca56edcdec714e2ab933b664cdae51ed
Quelldatensatz
uspto-grants-2008_11
Patentnummer
US07456203B2

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