تفاعل #2320

ord-a4c192010f8d498c9feb99faee7fc4d5

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
4°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITwas continued overnight at ambient temperature
  2. 2
    أخرىThe solvent was evaporated in vacuo
  3. 3
    أخرىthe residue partitioned between ethyl acetate and water
  4. 4
    استخلاصThe aqueous phase was re-extracted with further ethyl acetate
  5. 5
    غسيلthe combined organic extracts washed with water and brine
  6. 6
    تجفيفdried (MgSO4)
  7. 7
    أخرىevaporated

الإجراء التجريبي

Sodium hydride (50% w/w dispersion in mineral oil, 3.7 g) was treated under argon with repeated washes of hexane. The oil-free residue was suspended in dry DMF (100 ml) and 4-hydroxyphenylacetic acid (13.0 g) was added portionwise to the stirred cooled (4° C.) mixture. After 30 minutes, benzyl bromide (9.2 ml) was added dropwise and, after a further 1 hour at 4° C., stirring was continued overnight at ambient temperature. The solvent was evaporated in vacuo and the residue partitioned between ethyl acetate and water. The aqueous phase was re-extracted with further ethyl acetate and the combined organic extracts washed with water and brine, then dried (MgSO4) and evaporated. The crystalline residue gave benzyl 4-hydroxyphenylacetate, 17.8 g, as off-white crystals: m.p. 70°-72° C.; NMR (CDCl3) δ 7.32(5H, m), 7.14(2H, d), 6.76(2H, d), 5.12(2H, s), 3.59(2H, s); m/e 242 (M.)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05728701uspto-grants-1998_03