تفاعل #320787

ord-716fca5737634edf92985c70a3636402

معادلة التفاعل

CC1(C)Cc2c(Br)cccc2O1
4-bromo-2,3-dihydro-2,2-dimethylbenzofuran
O=S(=O)([O-])OOS(=O)(=O)[O-].[K+].[K+]
potassium persulfate
CC1(C)Oc2cccc(Br)c2C1=O
4-bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranone
المردود 67.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةat reflux for one hour
  2. 2
    استخلاصThe mixture is then extracted with one 200 mL portion of diethyl ether
  3. 3
    تجفيفThe extract is dried with magnesium sulfate
  4. 4
    ترشيحfiltered
  5. 5
    تركيزThe filtrate is concentrated under reduced pressure to a residual oil
  6. 6
    غسيلElution
  7. 7
    تركيزconcentrated under reduced pressure

الإجراء التجريبي

Under a nitrogen atmosphere, a stirred solution of 3.0 grams (0.013 mole) 4-bromo-2,3-dihydro-2,2-dimethylbenzofuran, 10.7 grams (0.039 mole) of potassium persulfate, and 3.3 grams (0.013 mole) of copper(II) sulfate pentahydrate in 30 mL of water and 30 mL of acetonitrile is heated at reflux for one hour. After this time the reaction mixture is poured into 200 mL of water. The mixture is then extracted with one 200 mL portion of diethyl ether. The extract is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residual oil. The oil is subjected to column chromatography on silica gel. Elution is accomplished using 1:1 petroleum ether and methylene chloride. The product-containing fractions are combined and concentrated under reduced pressure, yielding 2.1 grams of 4-bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranone. The NMR spectrum is consistent with the proposed structure.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05593998uspto-grants-1997_01