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Diethyl Ether → HCID 14183813、化合物

HRID 1484480
ノート
印刷プレビュー

反応式

HRID 1484480 の反応式
[OH:1][CH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:11])[C:7]([F:10])([F:9])[F:8].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.C([O-])(O)=O.[Na+].CCOCC>C(Cl)Cl>[O:1]=[CH:2][CH2:3][CH2:4][NH:5][C:6](=[O:11])[C:7]([F:9])([F:10])[F:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 3283Diethyl EtherHCID 159087TriacetoxyperiodinaneHCID 516892Sodium BicarbonateHCID 1987732N-(3-Hydroxypropyl)trifluoroacetamide

生成物 1

HCID 14183813HCID 14183813、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of N-(3-hydroxypropyl)trifluoroacetamide (1.6 g, 9.3 mmol) in anhydroud DCM (10 mL) cooled to 0° C. was added a solution of Dess-Martin periodinane (30 mL of 15 wt % in DCM; 14 mmol). Stirring was continued at 0° C. for 10 min, then the mixture was allowed to warm to room temperature and stirring was continued for 2 h. The mixture was poured onto a biphasic mixture of saturated aqueous NaHCO3 (60 mL) and Et2O (60 mL) and stirred vigorously for 20 min. The forming precipitate was eliminated by filtration and the layers separated. The aqueous layer was extracted with Et2O. The combined organic layers were washed with brine, dried (MgSO4), filtrated, and evaporated. The product was purified by column chromatography (Hex:EtOAc 3:2) to provide N-(3-oxopropyl)trifluoroacetamide as a viscous liquid in a yield of 0.82 g (52%). The product decomposes at room temperature and was used within 24 h of preparation. 1H-NMR (500 MHz, CDCl3): δ=2.84 ppm (t, J=6.0 Hz, 2H), 3.64 ppm (dt, J=6.0, 6.0 Hz, 2H), 6.98 ppm (bs, 1H), 9.81 ppm (s, 1H); 13C-NMR (500 MHz, CDCl3): δ=33.36, 42.58, 115.74 ppm (q, J=1144 Hz), 157.42 ppm (q, J=146.5 Hz), 200.85 ppm.

後処理

  1. stirringstirring
  2. waitwas continued for 2 h
  3. stirringstirred vigorously for 20 min
  4. filtrationThe forming precipitate was eliminated by filtration
  5. customthe layers separated
  6. extractionThe aqueous layer was extracted with Et2O
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried (MgSO4)
  9. filtrationfiltrated
  10. customevaporated
  11. customThe product was purified by column chromatography (Hex:EtOAc 3:2)

出典と根拠

ORDレコード
ord-b52a696e56f94e5a8cc7a4c4a79310cb
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09422232B2

反応ノート

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