تفاعل #11033

ord-072c3d9de7de4b1389dab342867a40c5

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
COC(=O)/C=C(\Oc1ccccc1[N+](=O)[O-])C(=O)OC
dimethyl 2-(2-nitrophenoxy)fumarate
COC(=O)/C=C(/Oc1ccccc1[N+](=O)[O-])C(=O)OC
dimethyl 2-(2-nitrophenoxy)maleate
COC(=O)c1cc(=O)c2cccc([N+](=O)[O-])c2o1
8-nitro-2-methoxycarbonyl-4-oxo-4H-1-benzopyran
المردود 86.0%

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA 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

A reaction container equipped with a stirrer, a cooling tube and a thermometer was charged with 300 parts by weight of chlorosulfonic acid. Thereto, 60 parts by weight of a mixture (content: 81.1% by weight, fumaric acid/maleic acid ratio=57/43) containing dimethyl 2-(2-nitrophenoxy)fumarate and dimethyl 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 60° C. and the mixture was stirred and kept at the same temperature for 5 hours and at an inner temperature of 70° C. for 3 hours to obtain a reaction solution containing 8-nitro-2-methoxycarbonyl-4-oxo-4H-1-benzopyran (reaction yield: 86%). After cooled to room temperature, the reaction solution was poured gradually into 360 parts by weight of water. The mixture was kept at an inner temperature of 60° C. for 8 hours and then cooled to an inner temperature of 0° C. gradually. Precipitated crystals were filtered and dried to obtain 30 parts by weight of a crystalline mixture of 8-nitro-2-methoxycarbonyl-4-oxo-4H-1-benzopyran and 8-nitro-2-carboxy-4-oxo-4H-1-benzopyran (the content of 8-nitro-2-methoxycarbonyl-4-oxo-4H-1-benzopyran: 2.5% by weight; the content of 8-nitro-2-carboxy-4-oxo-4H-1-benzopyran: 96.7% by weight). The yield of 8-nitro-2-methoxycarbonyl-4-oxo-4H-1-benzopyran was 2% and the yield of 8-nitro-2-carboxy-4-oxo-4H-1-benzopyran was 73%.

المصدر

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