تفاعل #81549

ord-a70620ce81214ac6a7dcb26b2b59ed24

معادلة التفاعل

O=C([O-])O.[Na+]
sodium bicarbonate
O=C(O)c1ccc(O)cc1
4-hydroxybenzoic acid
C=C(C)C
isobutylene
O=S(=O)(O)O
sulfuric acid
CC(C)(C)OC(=O)c1ccc(O)cc1
title product
CC(C)(C)OC(=O)c1ccc(O)cc1
4-Hydroxybenzoic acid tert-butyl ester

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe bomb was sealed
  2. 2
    درجة الحرارةthe reaction mixture was cooled to -78° C.
  3. 3
    استخلاصextracted with diethyl ether (2×50.0 mL)
  4. 4
    تركيزThe combined organic phases were concentrated
  5. 5
    أخرىthe residue chromatographed on silica gel (
  6. 6
    غسيلeluted with 5% methanol in methylene chloride

الإجراء التجريبي

To a solution of 4-hydroxybenzoic acid (2.00 g, 14.5 mmol) in 1,4-dioxane (10.0 mL) saturated with isobutylene at -78° C. in a metal bomb was added concentrated sulfuric acid (0.150 mL). The bomb was sealed and warmed to room temperature. After 72 hours at room temperature, the reaction mixture was cooled to -78° C., poured into saturated sodium bicarbonate (30.0 mL) and extracted with diethyl ether (2×50.0 mL). The combined organic phases were concentrated and the residue chromatographed on silica gel (eluted with 5% methanol in methylene chloride to give 290 mg (Y: 10%) of the title product; 1H-NMR (CDCl3): δ7.89 (d, J=8.8 Hz, 2H), 6.83 (d, J=8.8 Hz, 2H), 1.57 (s, 9H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05618839uspto-grants-1997_04