تفاعل #74934

ord-57d05772f0d3420799e83c85b730f450

معادلة التفاعل

S
hydrogen sulfide
S=P12SP3(=S)SP(=S)(S1)SP(=S)(S2)S3
phosphorus pentasulfide
S
hydrogen sulfide
[Na+].[OH-]
sodium hydroxide
COc1ccc(CC(=O)C(CC(=O)c2ccc(Cl)cc2)Cc2ccc(OC)cc2)cc1
1,2-di-p-anisyl-4-p-chlorophenylbutane-1,4-dione
COc1ccc(Cc2cc(-c3ccc(Cl)cc3)sc2Cc2ccc(OC)cc2)cc1
2,3-di-p-anisyl-5-p-chlorophenylthiophene
المردود 153.3%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe autoclave was cooled with a Dry Ice-acetone bath
  2. 2
    درجة الحرارةheated for three hours at 162°-168° C. (1220-1290 psig)
  3. 3
    أخرىTreatment with 150 ml of absolute ethanol to remove unreacted phosphorus pentasulfide
  4. 4
    أخرىgave 77 g of crude product
  5. 5
    أخرىRecrystallization from 400 ml of absolute ethanol

الإجراء التجريبي

In a 1-liter stainless steel autoclave equipped with stirrer were placed 54.5 g (0.133 mole) of 1,2-di-p-anisyl-4-p-chlorophenylbutane-1,4-dione, 100 ml of xylene and 30 g (0.0675 mole) of phosphorus pentasulfide. The autoclave was cooled with a Dry Ice-acetone bath and 130 g (3.81 moles) of hydrogen sulfide was distilled into the autoclave. The vessel was stirred and heated for three hours at 162°-168° C. (1220-1290 psig). After cooling to room temperature the hydrogen sulfide was vented into an aqueous sodium hydroxide solution. Treatment with 150 ml of absolute ethanol to remove unreacted phosphorus pentasulfide gave 77 g of crude product. Recrystallization from 400 ml of absolute ethanol gave 45 g (83.1%) of pure 2,3-di-p-anisyl-5-p-chlorophenylthiophene, m.p. 125°-128° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04174405uspto-grants-1979_11