تفاعل #88832

معادلة التفاعل

isopropyl acetate

4-fluoro-2-(trifluoromethyl)benzoyl chloride

6-amino-3,3-dimethyl-3H-benzo[c][1,2]oxaborol-1-ol

6-amino-3,3-dimethyl-3H-benzo[c][1,2]oxaborol-1-ol

K2CO3

→

4-fluoro-N-(1-hydroxy-3,3-dimethyl-1,3-dihydro-benzo[c][1,2]oxaborol-6-yl)-2-trifluoromethyl benzamide

المردود 113.1%

المذيبات

water

water

THF

acetone

water

ظروف التفاعل

المعالجة

1. 1
   أخرىA 22 L four-necked round-bottomed-flask equipped with a nitrogen inlet adapter, mechanical stirrer
2. 2
   workup.WAITThe resulting suspension was aged for 24 h at room temperature
3. 3
   workup.ADDITIONwas added
4. 4
   workup.WAITAfter 30 min
5. 5
   أخرىthe phases were partitioned
6. 6
   استخلاصThe organic phase was further extracted with water (2.8 L)
7. 7
   تجفيفThe organic phase was dried over MgSO4
8. 8
   تركيزconcentrated in vacuo
9. 9
   أخرىto provide a tan solid
10. 10
    workup.STIRRINGthe mixture was stirred for 30 min
11. 11
    أخرىto produce a seed bed
12. 12
    workup.STIRRINGThe suspension was stirred at room temperature overnight
13. 13
    أخرىthe solids were collected on a frit
14. 14
    غسيلThe cake was rinsed with 1:1 acetone/water (1.0 L) and air
15. 15
    أخرىdried to constant weight

الإجراء التجريبي

A 22 L four-necked round-bottomed-flask equipped with a nitrogen inlet adapter, mechanical stirrer and thermocouple was charged with 6-amino-3,3-dimethyl-3H-benzo[c][1,2]oxaborol-1-ol (554 g, 3.13 mol), THF (5.5 L, anhydrous, stabilizer free) and K2CO3 (865 g, 6.26 mol). The suspension was stirred at room temperature for 30 min and 4-fluoro-2-(trifluoromethyl)benzoyl chloride (780 g, 3.44 mol) was added over 30 min. The resulting suspension was aged for 24 h at room temperature. HPLC showed unreacted 6-amino-3,3-dimethyl-3H-benzo[c][1,2]oxaborol-1-ol so an additional 42 mL of the acid chloride was added. After 30 min, water (2.8 L) and isopropyl acetate (5.5 L) were added and the phases were partitioned. The organic phase was further extracted with water (2.8 L) and then brine (2.8 L). The organic phase was dried over MgSO4 and concentrated in vacuo to provide a tan solid. The solid was dissolved with acetone (3.0 L) and transferred to a mechanically stirred 50 L round-bottomed-flask. Distilled water (2.0 L) was added in one portion and the mixture was stirred for 30 min to produce a seed bed and then additional water (1.0 L) was added over 30 min. The suspension was stirred at room temperature overnight and the solids were collected on a frit. The cake was rinsed with 1:1 acetone/water (1.0 L) and air dried to constant weight to provide 4-fluoro-N-(1-hydroxy-3,3-dimethyl-1,3-dihydro-benzo[c][1,2]oxaborol-6-yl)-2-trifluoromethyl benzamide as a dark tan solid (1.3 kg).

المصدر