Triethylamine → Ethyl 5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazole-3-carboxylate

HRID 1827887

反応式

HRID 1827887 の反応式
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[CH2:10])=[CH:5][CH:4]=1.Cl[CH:14]([NH:20][OH:21])[C:15]([O:17][CH2:18][CH3:19])=[O:16].C(N(CC)CC)C>C1COCC1>[F:1][C:2]([F:11])([F:12])[C:3]1[CH:4]=[CH:5][C:6]([CH:9]2[O:21][N:20]=[C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:10]2)=[CH:7][CH:8]=1

参加物

5

実験手順

To a mixture of 1-(trifluoromethyl)-4-vinylbenzene (2.0 g, 11.27 mmol), a compound of formula (20) and ethyl 2-chloro-2-(hydroxyamino)acetate (2.11 g, 13.52 mmol), a compound of formula (21), in anhydrous THF was added a solution of triethylamine (3.0 ml) in tetrahydrofuran was added dropwise at room temperature. The mixture was stirred overnight under N2. The white precipitate thus formed was filtered off, and washed twice with tetrahydrofuran (10 ml). The solvent was removed from the filtrate under reduced pressure, and the residue partitioned between water/ethyl acetate (20 ml:20 ml v/v), extracting three times with 20 ml of ethyl acetate. The combined organic layers were washed with aqueous ammonium chloride, and dried over MgSO4, to provide ethyl 5-[4-(trifluoromethyl)phenyl]-4,5-dihydroisoxazole-3-carboxylate, a compound of formula (22).

後処理

  1. additionwas added dropwise at room temperature
  2. customThe white precipitate thus formed
  3. filtrationwas filtered off
  4. washwashed twice with tetrahydrofuran (10 ml)
  5. customThe solvent was removed from the filtrate under reduced pressure
  6. customthe residue partitioned between water/ethyl acetate (20 ml:20 ml v/v)
  7. extractionextracting three times with 20 ml of ethyl acetate
  8. washThe combined organic layers were washed with aqueous ammonium chloride
  9. dry with materialdried over MgSO4

出典と根拠

ORDレコード
ord-4fa9d205e4504e8882f4f8c13f3d8b56
出典データセット
uspto-grants-2006_06
特許番号
US07056924B2

関連ノート

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