تفاعل #1563875

ord-fac823e27f7d4f01835b164bc872d328

معادلة التفاعل

C=[N+]=[N-]
diazomethane
O=C(Cl)c1ccco1
furan-2-carbonyl chloride
C=[N+]=[N-]
diazomethane
[N-]=[N+]=CC(=O)c1ccco1
2-diazo-1-(furan-2-yl)ethanone
المردود 49.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تجفيفdried over KOH
  2. 2
    درجة الحرارةthe resulting ethereal solution was cooled in an ice-salt bath
  3. 3
    أخرىThe solvent was evaporated to dryness (under an argon atmosphere
  4. 4
    أخرىthe water bath temperature below 25° C.
  5. 5
    أخرىwas purified by column chromatography
  6. 6
    أخرىEvaporation of solvent

الإجراء التجريبي

N-Nitroso-N-methylurea (16.14 g, 61.53 mmol) was treated with a concentrated NaOH aqueous solution to produce diazomethane. The diazomethane was combined with dry ether (100 ml), dried over KOH, and the resulting ethereal solution was cooled in an ice-salt bath. A solution of furan-2-carbonyl chloride (1.6 g, 12.3 mmol) in dry ether (25 ml) was then added very slowly to the diazomethane solution. The reaction mixture was stirred overnight at room temperature. The solvent was evaporated to dryness (under an argon atmosphere, and keeping the water bath temperature below 25° C.), and the resulting crude material was purified by column chromatography using 230-400 mesh silica gel and 1% triethylamine in DCM solvent system. Evaporation of solvent yielded 2-diazo-1-(furan-2-yl)ethanone as a yellow oil (900 mg, 49%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09402397B2uspto-grants-2016_08