반응 #2358489

ord-701126159e044d88a57218f1a9553e71

반응 방정식

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
수율 96.2%

용매

반응 조건

온도
75°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction mixture was cooled to room temperature
  2. 2
    농축concentrated under reduced pressure
  3. 3
    workup.ADDITIONTo the obtained residue was added water
  4. 4
    세척washed with tert-butyl methyl ether 3 times
  5. 5
    workup.ADDITIONTo the aqueous layer was added concentrated hydrochloric acid
  6. 6
    추출extracted with tert-butyl methyl ether 3 times
  7. 7
    세척The combined organic layer was washed with saturated aqueous sodium chloride solution
  8. 8
    건조dried over magnesium sulfate
  9. 9
    농축concentrated under reduced pressure

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09119396B2uspto-grants-2015_09