Réaction #5465

Équation de réaction

sodium hydride

ethyl mercaptan

4-amino-5-chloro-2-methoxybenzoic acid

→

white solid

Rendement 83.4%

4-Amino-5-chloro-2-hydroxybenzoic acid

Rendement 83.4%

Solvants

dimethylformamide

Conditions de réaction

Traitement

1. 1
   TempératureA cooled
2. 2
   Températureto maintain a pot temperature below 15° C.
3. 3
   Températurecooled (5° C.)
4. 4
   TempératureThe mixture was heated to 105°±5° C. for 4 hours
5. 5
   Températurecooled
6. 6
   Concentrationconcentrated in vacuo
7. 7
   Autreto remove most of the dimethylformamide
8. 8
   ExtractionThe aqueous solution was extracted with methylene chloride (2×150 mL), and ether (150 mL)
9. 9
   Filtrationfiltered
10. 10
    Lavagethe filter cake washed with water
11. 11
    Autredried in vacuo
12. 12
    Autreto afford 35.7 g of crude product
13. 13
    AutreCrystallization from tetrahydrofuran/hexane

Mode opératoire

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.

Source