反応 #5465

ord-b8ad3a760b1242ffb810507057579d5e

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度A cooled
  2. 2
    温度to maintain a pot temperature below 15° C.
  3. 3
    温度cooled (5° C.)
  4. 4
    温度The mixture was heated to 105°±5° C. for 4 hours
  5. 5
    温度cooled
  6. 6
    濃縮concentrated in vacuo
  7. 7
    その他to remove most of the dimethylformamide
  8. 8
    抽出The aqueous solution was extracted with methylene chloride (2×150 mL), and ether (150 mL)
  9. 9
    ろ過filtered
  10. 10
    洗浄the filter cake washed with water
  11. 11
    その他dried in vacuo
  12. 12
    その他to afford 35.7 g of crude product
  13. 13
    その他Crystallization from tetrahydrofuran/hexane

実験手順

A cooled (5° C.) suspension of 60% sodium hydride/oil dispersion (20.0 g, 0.50 mole) in anhydrous dimethylformamide (300 mL) under nitrogen was treated slowly dropwise with ethyl mercaptan (18.7 g, 0.30 mole) so as to maintain a pot temperature below 15° C., then stirred at room temperature for 15 minutes, cooled (5° C.), and treated in portions with 4-amino-5-chloro-2-methoxybenzoic acid (40.33 g, 0.20 mole). The mixture was heated to 105°±5° C. for 4 hours, cooled, and concentrated in vacuo to remove most of the dimethylformamide, then plunged into water (500 mL). The aqueous solution was extracted with methylene chloride (2×150 mL), and ether (150 mL), acidified with concentrated HCl (55 mL), filtered, and the filter cake washed with water and dried in vacuo to afford 35.7 g of crude product. Crystallization from tetrahydrofuran/hexane afforded 31.3 g (83%) of white solid; mp 192° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05244907uspto-grants-1993_09