Hydrochloric Acid → 5-[(2-Methoxyethoxy)methyl]-1,3-thiazole-2-carbaldehyde

HRID 1881880노트

반응식

HRID 1881880 반응식
[O:1]1CCO[CH:2]1[C:6]1[S:7][C:8]([CH2:11][O:12][CH2:13][CH2:14][O:15][CH3:16])=[CH:9][N:10]=1.Cl.C(=O)([O-])O.[Na+]>CC(C)=O>[CH3:16][O:15][CH2:14][CH2:13][O:12][CH2:11][C:8]1[S:7][C:6]([CH:2]=[O:1])=[N:10][CH:9]=1

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 593316232-(1,3-Dioxolan-2-yl)-5-[(2-methoxyethoxy)methyl]-1,3-thiazole

생성물 1

HCID 593313455-[(2-Methoxyethoxy)methyl]-1,3-thiazole-2-carbaldehyde수율 81%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A mixture of 2-(1,3-dioxolan-2-yl)-5-[(2-methoxyethoxy)methyl]-1,3-thiazole (0.40 g), 1M hydrochloric acid (2 mL) and acetone (10 mL) was stirred with heating under reflux for 4 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography, and the title compound (0.26 g, yield 81%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (3:1, volume ratio).

후처리

  1. temperaturewith heating
  2. temperatureunder reflux for 4 hr
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe ethyl acetate layer was washed with saturated brine
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-98719fe730c84549a0accb5768b49e35
출처 데이터셋
uspto-grants-2012_11
특허 번호
US08318746B2

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