Ammonium fluoride → Ethyl 8-allyl-6-(trifluoromethoxy)-2-(trifluoromethyl)-2h-chromene-3-carboxylate

HRID 854918ノート

反応式

HRID 854918 の反応式
I[C:2]1[CH:3]=[C:4]([O:21][C:22]([F:25])([F:24])[F:23])[CH:5]=[C:6]2[C:11]=1[O:10][CH:9]([C:12]([F:15])([F:14])F)[C:8]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:7]2.[CH2:26]([CH:30]([Sn])C=C(CCCC)CCCC)[CH2:27]CC.[NH4+].[F-:43]>C1(C)C=CC=CC=1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:30]([C:2]1[CH:3]=[C:4]([O:21][C:22]([F:25])([F:24])[F:23])[CH:5]=[C:6]2[C:11]=1[O:10][CH:9]([C:12]([F:14])([F:15])[F:43])[C:8]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:7]2)[CH:26]=[CH2:27]

参加物

6

実験手順

To a mixture of ethyl 8-iodo-6-(trifluoromethoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylate prepared as in Example 21a, Step 2 (1.00 g, 2.07 mmole) and Pd(PPh3)4 (0.239 g, 0.207 mmole) in anhydrous toluene (50 mL) under a dry N2 atmosphere was added tributylallyltin (0.707 mL, 2.28 mmole). The mixture was refluxed for 16 h and 20% NH4F solution (50 mL) was added. The mixture was stirred for 1 h and extracted with EtOAc (200 mL). The extract was washed with brine (100 mL), dried over Na2SO4, filtered and concentrated in vacuo. Purification by silica chromatography (9:1 hexanes:EtOAc) gave 0.770 g (94% yield) of the product as a yellow oil: EIHRMS m/z 396.0769 (M+, C17H14F6O4, Calc'd 396.0796).

後処理

  1. temperatureThe mixture was refluxed for 16 h
  2. extractionextracted with EtOAc (200 mL)
  3. washThe extract was washed with brine (100 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customPurification by silica chromatography (9:1 hexanes:EtOAc)

出典と根拠

ORDレコード
ord-c7396466f8424b1b8561efa7db04ad2e
出典データセット
uspto-grants-2007_08
特許番号
US07259266B2

反応ノート

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