Water → O-(2-methoxybenzyl)-6-dimethylaminohexanol

HRID 272796

반응식

HRID 272796 반응식
[CH3:1][N:2]([CH3:10])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][OH:9].[H-].[Na+].O.[CH3:14][O:15][C:16]1[CH:23]=[CH:22][CH:21]=[CH:20][C:17]=1[CH2:18]Cl>O1CCCC1>[CH3:14][O:15][C:16]1[CH:23]=[CH:22][CH:21]=[CH:20][C:17]=1[CH2:18][O:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][N:2]([CH3:10])[CH3:1]

참가 물질

6

실험 절차

6-(Dimethylamino)hexanol (8.80 g, 60.6 mmol) was dissolved in an anhydrous 2:1 mixture of tetrahydrofuran and dimethylfornamide (150 mL) and the solution was cooled in an ice bath. Sodium hydride (60% in oil, 3.23 g, 80.8 mmol) was added in portions and after 5 min. the water bath was removed. After 45 min., 2-methoxybenzyl chloride (6.28 g, 40.4 mmol) was added. After 4 h, the reaction mixture was quenched with 1 M sodium thiosulfate and tetrahydrofuran was removed in vacuo. The reaction mixture was washed with ethyl acetate and the aqueous phase was basified with 3 M sodium hydroxide, followed by extraction with ether. The ether layer was dried over potassium carbonate, filtered and acidified with 4 M hydrochloric acid in dioxane. The reaction mixture was concentrated in vacuo and the residue was crystallized form ethanol/ether to give O-(2-methoxybenzyl)-6-dimethylaminohexanol as the hydrochloride salt (10.4 g, 85%). MS (M-Cl)+266.3.

후처리

  1. temperaturethe solution was cooled in an ice bath
  2. customwas removed
  3. waitAfter 4 h
  4. customthe reaction mixture was quenched with 1 M sodium thiosulfate and tetrahydrofuran
  5. customwas removed in vacuo
  6. washThe reaction mixture was washed with ethyl acetate
  7. extractionfollowed by extraction with ether
  8. dry with materialThe ether layer was dried over potassium carbonate
  9. filtrationfiltered
  10. concentrationThe reaction mixture was concentrated in vacuo
  11. customthe residue was crystallized form ethanol/ether

출처 및 근거

ORD 기록
ord-6aff08e24c004d02b3a693f66a0b9f8b
출처 데이터셋
uspto-grants-2008_11
특허 번호
US07456203B2

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