تفاعل #56367

ord-2fd7dae8e4484fd9b44ed2b20e463ff2

معادلة التفاعل

O=C(c1ccccc1-c1ccccc1)C(O)c1ccccc1
phenylbenzoin
O=C(c1ccccc1-c1ccccc1)C(O)c1ccccc1
phenylbenzoin
NO
hydroxylamine
CC(=O)[O-].[Na+]
sodium acetate
Cl.NO
hydroxylamine hydrochloride
NO
hydroxylamine
O=C(c1ccccc1-c1ccccc1)C(O)c1ccccc1
phenylbenzoin
ON=C(c1ccccc1)C(O)(c1ccccc1)c1ccccc1
alpha-phenylbenzoin oxime
المردود 40.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىround bottomed flask fitted with a reflux condenser
  2. 2
    أخرىwas prepared
  3. 3
    workup.ADDITIONby treating 177.9 g
  4. 4
    workup.ADDITIONwas added
  5. 5
    درجة الحرارةThe solution was cooled
  6. 6
    ترشيحfiltered
  7. 7
    workup.ADDITIONtreated with refluxing hexane
  8. 8
    workup.WAITAfter 72 hours the solid remaining in the extraction thimble
  9. 9
    أخرىwas collected

الإجراء التجريبي

180 g (0.625 mole) of phenylbenzoin was added to a 3 liter, one necked, round bottomed flask fitted with a reflux condenser and a nitrogen bypass. 1.45 liters of methanol was added to dissolve the phenylbenzoin and free hydroxylamine was prepared by treating 177.9 g. (2.56 moles) hydroxylamine hydrochloride with 209.9 g (2.56 moles) of sodium acetate in water. The resultant solution was added to the phenylbenzoin and the reaction mixture was stirred for 48 hours at reflux at which time an additional 1.24 moles of hydroxylamine was added. The solution was cooled and filtered. The solids were then placed in a Soxhlet extractor and treated with refluxing hexane. After 72 hours the solid remaining in the extraction thimble was collected to yield 40% of the theoretical yield of pure alpha-phenylbenzoin oxime, m.p. 150°-52° C. (lit. 153.5) The hexane extract can be concentrated to yield unreacted phenylbenzoin (50% of theory) which may be recycled to afford additional phenylbenzoin oxime. This material was employed to polymerize 2,6-xylenol using the following composition:

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04225528uspto-grants-1980_09