Water → 1-(7-Amino-2,3-dihydro-1,4-benzodioxin-6-yl)-2-chloroethan-1-one

HRID 411846

反応式

HRID 411846 の反応式
[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([NH2:11])=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1.B(Cl)(Cl)Cl.[Cl:16][CH2:17][C:18]#N.[Cl-].[Ga+3].[Cl-].[Cl-].[OH2:24]>ClCCl>[NH2:11][C:9]1[C:8]([C:18](=[O:24])[CH2:17][Cl:16])=[CH:7][C:6]2[O:1][CH2:2][CH2:3][O:4][C:5]=2[CH:10]=1

参加物

7

実験手順

1,4-benzodioxan-6-amine, Formula VIII, (160 g, 1.06 mol) is dissolved in dichloromethane (DCM, 2.4 L) and cooled in an ice bath to less than 10° C. Boron trichloride gas (150 g, 1.27 mol, 1.2 eq) is added over 0.75 hour. The resulting brown slurry is then stirred overnight at room temperature. The slurry is then cooled in an ice bath to 10° C. and chloroacetonitrile (94 mL, 1.48 mol, 1.4 eq) is added in one portion. Gallium chloride (205 g, 1.16 mol, 1.1 eq) is dissolved in DCM (310 mL) and added to the reaction over 0.5 h. The resulting brown slurry is then heated at reflux overnight (13-24 h). The brown solution is then cooled to rt and poured into a stirred mixture or DCM (6.4 L)) and water (6.4 L). The mixture is stirred for 1.5 to 2 h to allow the solids to dissolve. The layers are then separated and the aqueous phase is extracted with DCM (2 L). The organic layers are combined and concentrated under vacuum (about 100 mm Hg) to about 320 mL. (Crystallization occurs during the concentration.) Heptane (640 mL) is added over 1 hour and the slurry stirred overnight at room temperature. The slurry is filtered, washing the cake with heptane (200 mL). The cake is then dried overnight at 40° C. under high vacuum (about 1 mm Hg) to give 206 g (86%) of 1-(7-amino-2,3-dihydro-benzo[1,4]dioxin-6-yl)-2-chloro-ethanone as a yellow solid.

後処理

  1. temperaturecooled in an ice bath to less than 10° C
  2. temperatureThe slurry is then cooled in an ice bath to 10° C.
  3. additionadded to the reaction over 0.5 h
  4. temperatureThe resulting brown slurry is then heated
  5. temperatureat reflux overnight (13-24 h)
  6. temperatureThe brown solution is then cooled to rt
  7. stirringThe mixture is stirred for 1.5 to 2 h
  8. dissolutionto dissolve
  9. customThe layers are then separated
  10. extractionthe aqueous phase is extracted with DCM (2 L)
  11. concentrationconcentrated under vacuum (about 100 mm Hg) to about 320 mL
  12. custom(Crystallization
  13. concentrationoccurs during the concentration
  14. addition) Heptane (640 mL) is added over 1 hour
  15. stirringthe slurry stirred overnight at room temperature
  16. filtrationThe slurry is filtered
  17. washwashing the cake with heptane (200 mL)
  18. customThe cake is then dried overnight at 40° C. under high vacuum (about 1 mm Hg)

出典と根拠

ORDレコード
ord-f07d36d79fcc43b79b904761199dfdc3
出典データセット
uspto-grants-2003_05
特許番号
US06559309B2

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