تفاعل #2358489

ord-701126159e044d88a57218f1a9553e71

معادلة التفاعل

COC(=O)c1cc2cc(C(F)(F)F)ccc2s1
methyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate
O.[Li+].[OH-]
lithium hydroxide monohydrate
O
water
O=C(O)c1cc2cc(C(F)(F)F)ccc2s1
5-(trifluoromethyl)benzo[b]thiophene-2-carboxylic acid
المردود 96.2%

المذيبات

ظروف التفاعل

درجة الحرارة
75°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was cooled to room temperature
  2. 2
    تركيزconcentrated under reduced pressure
  3. 3
    workup.ADDITIONTo the obtained residue was added water
  4. 4
    غسيلwashed with tert-butyl methyl ether 3 times
  5. 5
    workup.ADDITIONTo the aqueous layer was added concentrated hydrochloric acid
  6. 6
    استخلاصextracted with tert-butyl methyl ether 3 times
  7. 7
    غسيلThe combined organic layer was washed with saturated aqueous sodium chloride solution
  8. 8
    تجفيفdried over magnesium sulfate
  9. 9
    تركيزconcentrated under reduced pressure

الإجراء التجريبي

A mixture of 10.0 g of methyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, 1.80 g of lithium hydroxide monohydrate, 30 ml of water and 90 ml of methanol was stirred at 75° C. for 1 hour. The reaction mixture was cooled to room temperature and then concentrated under reduced pressure. To the obtained residue was added water, and washed with tert-butyl methyl ether 3 times. To the aqueous layer was added concentrated hydrochloric acid, and then extracted with tert-butyl methyl ether 3 times. The combined organic layer was washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, and then concentrated under reduced pressure to obtain 9.10 g of 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylic acid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09119396B2uspto-grants-2015_09