Sodium ethoxide → 2,3-dihydro-6-fluoro-4-cyano-2-(2-phenylethyl)-4H-1-benzopyran

HRID 2248293노트

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HRID 2248293 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH:9]([CH2:11][CH2:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH2:8][C:7](=O)[C:6]=2[CH:20]=1.C1(C)C(S([CH2:30][N+:31]#[C-])(=O)=O)=CC=CC=1.[O-]CC.[Na+].[Na]>O1CCCC1.C(O)C>[C:30]([CH:7]1[C:6]2[CH:20]=[C:2]([F:1])[CH:3]=[CH:4][C:5]=2[O:10][CH:9]([CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:8]1)#[N:31]

참가 물질

7

반응물 4

HCID 2723922Sodium ethoxideHCID 5360545SodiumHCID 190944442,3-dihydro-6-fluoro-2-(2-phenylethyl)-4H-1-benzopyran-4-oneHCID 53627694Toluenesulfonylmethyl isocyanide

생성물 1

HCID 190944432,3-dihydro-6-fluoro-4-cyano-2-(2-phenylethyl)-4H-1-benzopyran수율 29.1%

시약·촉매·용매 2

HCID 702Ethanol용매2회HCID 8028Tetrahydrofuran용매

실험 절차

2,3-dihydro-6-fluoro-2-(2-phenylethyl)-4H-1-benzopyran-4-one (8.9 gm) was dissolved in anhydrous tetrahydrofuran, and toluenesulfonylmethylisocyanide (12.9 gm) added, followed by freshly prepared sodium ethoxide in ethanol (prepared from sodium (1.5 gm) in ethanol (60 mL) and the mixture stirred at room temperature overnight. The mixture was then concentrated in vacuo, and the residue partitioned between ethyl acetate and H2O, and the organic layer washed with H2O, brine, dried, filtered and evaporated. The residue was purified by column chromatography (2:1 hexanes/diethyl ether) to yield 4-cyano-2,3-dihydro-6-fluoro-2-(2-phenylethyl)-4H-1-benzopyran (2.7 gm, ir: 2250 cm-1).

후처리

  1. concentrationThe mixture was then concentrated in vacuo
  2. customthe residue partitioned between ethyl acetate and H2O
  3. washthe organic layer washed with H2O, brine
  4. customdried
  5. filtrationfiltered
  6. customevaporated
  7. customThe residue was purified by column chromatography (2:1 hexanes/diethyl ether)

출처 및 근거

ORD 기록
ord-dcc432068a9e4d18b8acd0795b0e2e87
출처 데이터셋
uspto-grants-1991_08
특허 번호
US05039672

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