반응 #74934

ord-57d05772f0d3420799e83c85b730f450

반응 방정식

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
수율 153.3%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04174405uspto-grants-1979_11