تفاعل #74187

ord-9f2baa41f5394f648cf574a825322f83

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate (2×100 ml)
  2. 2
    تجفيفThe combined organic extracts are dried over magnesium sulphate
  3. 3
    ترشيحfiltered
  4. 4
    أخرىevaporated under reduced pressure
  5. 5
    أخرىto give an orange oil
  6. 6
    workup.DISTILLATIONThe crude product is distilled under reduced pressure

الإجراء التجريبي

Into a 250 ml round bottom flask containing the bicyclo[3.2.1]octane-2,4-dione (10 g, 72 mmol) is added dry dichloromethane (100 ml) and pyridine (6.28 g, 87 mmol). To the stirred mixture is added dropwise over a period of 15 minutes the chloroacetyl chloride (9.82 g, 72 mmol) diluted in dichloromethane (100 ml). The reaction mixture is therefore stirred for 2 hours at room temperature. The reaction mixture is therefore poured into 100 ml of aqueous 2N HCl and extracted with ethyl acetate (2×100 ml). The combined organic extracts are dried over magnesium sulphate, filtered and evaporated under reduced pressure to give an orange oil. The crude product is distilled under reduced pressure to give chloro-acetic acid 4-oxo-bicyclo[3.2.1]oct-2-en-2-yl ester (13.4 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08541594B2uspto-grants-2013_09