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Sulfuric Acid → 5-Diethylphosphono-2-thiophenecarboxaldehyde

HRID 1431005
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HRID 1431005 반응식
[CH2:1]([O:3][P:4]([C:9]1[S:10][C:11]([CH:14]2N(C)CCN2C)=[CH:12][CH:13]=1)(=[O:8])[O:5][CH2:6][CH3:7])[CH3:2].S(=O)(=O)(O)[OH:22]>O>[CH2:6]([O:5][P:4]([C:9]1[S:10][C:11]([CH:14]=[O:22])=[CH:12][CH:13]=1)(=[O:8])[O:3][CH2:1][CH3:2])[CH3:7]
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참가 물질

4

반응물 2

HCID 1118Sulfuric AcidHCID 86659557[5-(1,3-Dimethyl-imidazolidin-2-yl)-thiophen-2-yl]-phosphonic acid diethyl ester

생성물 1

HCID 222749525-Diethylphosphono-2-thiophenecarboxaldehyde수율 48.3%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

To a solution of [5-(1,3-dimethyl-imidazolidin-2-yl)-thiophen-2-yl]-phosphonic acid diethyl ester (17.2 g, 60.17 mmol) in water (20 ml) was added sulfuric acid (3 ml) over 5 mins. The reaction was stirred at r.t. for 20 min, diluted with water, extracted with EtOAc. The organic layer was washed with sat. NaHCO3, dried over MgSO4, filtrated, concentrated, purified by Biotage (80% EtOAc) to give (5-formyl-thiophen-2-yl)-phosphonic acid diethyl ester (7.2 g, 48.3%). 1H NMR (300 MHz, DMSO-d6): δ 10.02 (d, J=2.4 Hz, 1H), 8.09 (m, 1H), 7.75 (m, 1H), 4.05 (m, 4H), 1.24 (m, 6H). LC-MS m/z=249.4 [C9H13O4PS+H]+.

후처리

  1. extractionextracted with EtOAc
  2. washThe organic layer was washed with sat. NaHCO3
  3. dry with materialdried over MgSO4
  4. filtrationfiltrated
  5. concentrationconcentrated
  6. custompurified by Biotage (80% EtOAc)

출처 및 근거

ORD 기록
ord-3d6befb08a0d4d87a810554f793458a6
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08940927B2

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