تفاعل #6629

ord-906733f298d349598a10f27ec82e8d53

معادلة التفاعل

CC(C)=CC(SC(C=C(C)C)c1ccccc1)c1ccccc1
phenyl-3-methylbut-2-enylsulfide
CC(C)=CC(SC(C=C(C)C)c1ccccc1)c1ccccc1
Compound 60
CC(C)=CC(SC(C=C(C)C)c1ccccc1)c1ccccc1
phenyl-3-methylbut-2-enylsulfide
O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3
phosphorus pentoxide
O=P(O)(O)O
phosphoric acid
c1ccccc1
benzene
CC1(C)CCSc2ccccc21
title compound
CC1(C)CCSc2ccccc21
4,4-Dimethylthiochroman

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThis solution was refluxed
  2. 2
    أخرىThe supernatant organic layer was decanted
  3. 3
    استخلاصthe syrupy residue extracted with 3×50ml ether
  4. 4
    غسيلwashed with water, saturated NaHCO3 and saturated NaCl solutions
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    أخرىSolvent was removed in vacuo
  7. 7
    workup.DISTILLATIONthe residue purified by kugelrohr distillation (80 degrees C., 0.5mm)

الإجراء التجريبي

To a solution of 15.48g (86.824 mmol) of phenyl-3-methylbut-2-enylsulfide (Compound 60) in 160ml benzene were added successively 12.6g (88.767mmol) of phosphorus pentoxide and 11 ml of 85% phosphoric acid. This solution was refluxed with vigorous stirring under argon for 20 hours, then cooled to room temperature. The supernatant organic layer was decanted and the syrupy residue extracted with 3×50ml ether. Organic fractions were combined and washed with water, saturated NaHCO3 and saturated NaCl solutions and then dried (MgSO4). Solvent was removed in vacuo and the residue purified by kugelrohr distillation (80 degrees C., 0.5mm) to give the title compound as a pale yellow oil. PMR (CDCl3) :& 1.30 (6H, s), 1.90-1.95 (2H, m), 2.95-3.00 (2H, m), 6.96-7.00 (2H, m), 7.04-7.07 (1H, m), 7.30-7.33 (1H, m).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05248777uspto-grants-1993_09