反应 #5465

ord-b8ad3a760b1242ffb810507057579d5e

反应方程式

[H-].[Na+]
sodium hydride
CCS
ethyl mercaptan
COc1cc(N)c(Cl)cc1C(=O)O
4-amino-5-chloro-2-methoxybenzoic acid
Nc1cc(O)c(C(=O)O)cc1Cl
white solid
收率 83.4%
Nc1cc(O)c(C(=O)O)cc1Cl
4-Amino-5-chloro-2-hydroxybenzoic acid
收率 83.4%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  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
    浓缩concentrated in vacuo
  7. 7
    其他to remove most of the dimethylformamide
  8. 8
    萃取The aqueous solution was extracted with methylene chloride (2×150 mL), and ether (150 mL)
  9. 9
    过滤filtered
  10. 10
    洗涤the filter cake washed with water
  11. 11
    其他dried in vacuo
  12. 12
    其他to afford 35.7 g of crude product
  13. 13
    其他Crystallization from tetrahydrofuran/hexane

实验过程

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.

来源

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