반응 #81548

ord-295ebae9a55f4da2ba964b92e6fd5bff

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과the solid filtered
  2. 2
    workup.DISSOLUTIONThe solid was dissolved in diethyl ether (40 mL)
  3. 3
    세척washed with saturated sodium bicarbonate (2×75 mL)
  4. 4
    건조The organic phase was then dried over anhydrous magnesium sulfate
  5. 5
    농축concentrated in vacuo

실험 절차

To a solution of terephthaloylchloride (2.00 g, 9.85 mmol) in dry pyridine (25.0 mL) was added tert-butyl alcohol (803 mg, 10.8 mmol). After 16 hours at 85° C. water (75.0 mL) was added and the solid filtered. The solid was dissolved in diethyl ether (40 mL) and washed with saturated sodium bicarbonate (2×75 mL). The organic phase was then dried over anhydrous magnesium sulfate and concentrated in vacuo to give 1.15 g (Y: 42%) of the title compound; 1H-NMR (CDCl3): δ8.01 (s, 4H), 1.60 (s, 18H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05618839uspto-grants-1997_04