تفاعل #11031

ord-82b9fddd628e4a618f9e86e30cf66450

معادلة التفاعل

O=S(=O)(O)Cl
chlorosulfonic acid
O=C(O)/C=C/C(=O)O.O=C(O)/C=C\C(=O)O
fumaric acid maleic acid
CCOC(=O)/C=C(\Oc1ccccc1[N+](=O)[O-])C(=O)OCC
diethyl 2-(2-nitrophenoxy)fumarate
CCOC(=O)/C=C(/Oc1ccccc1[N+](=O)[O-])C(=O)OCC
diethyl 2-(2-nitrophenoxy)maleate
CCOC(=O)c1cc(=O)c2cccc([N+](=O)[O-])c2o1
8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran
المردود 70.0%

ظروف التفاعل

درجة الحرارة
70°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter a reaction container equipped with a stirrer, a cooling tube
  2. 2
    workup.ADDITIONwas added dropwise at an inner temperature of 50° C. or below
  3. 3
    workup.ADDITIONAfter completion of addition
  4. 4
    أخرىto obtain a reaction solution

الإجراء التجريبي

After a reaction container equipped with a stirrer, a cooling tube and a thermometer was charged with 15 parts by weight of chlorosulfonic acid, 3 parts by weight of a mixture (content: 84.4% by weight, fumaric acid/maleic acid ratio=49/51) containing diethyl 2-(2-nitrophenoxy)fumarate and diethyl 2-(2-nitrophenoxy)maleate was added dropwise at an inner temperature of 50° C. or below. After completion of addition, the inner temperature was raised to 70° C. and the mixture was stirred and kept at the same temperature for 7 hours to obtain a reaction solution containing 8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran (reaction yield: 70%). After cooled to room temperature, the reaction solution was gradually added into 24 parts by weight of water. After kept at an inner temperature of 60° C. for 1 hour, the mixture was gradually cooled to an inner temperature of 0° C. Precipitated crystals were filtered and dried to obtain 1.3 parts by weight of a crystalline mixture containing 8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran and 8-nitro-2-carboxy-4-oxo-4H-1-benzopyran (the content of 8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran: 0.1% by weight; the content of 8-nitro-2-carboxy-4-oxo-4H-1-benzopyran: 86.4% by weight). The yield of 8-nitro-2-ethoxycarbonyl-4-oxo-4H-1-benzopyran was 0.1% and the yield of 8-nitro-2-carboxy-4-oxo-4H-1-benzopyran was 64%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07094914B2uspto-grants-2006_08