반응 #56135

ord-88ddb787963748189d79554a34ab2ab2

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled to 0° C.
  2. 2
    기타dropwise at 0°-5° C.
  3. 3
    workup.STIRRINGThe mixture is stirred for 2 hours at room temperature
  4. 4
    세척The organic phase is washed successively with water, dilute hydrochloric acid
  5. 5
    건조a 2% aqueous sodium bicarbonate solution, dried over sodium sulphate
  6. 6
    기타evaporated

실험 절차

20 g of 9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid are dissolved in 200 ml of tetrahydrofuran. After the addition of 5.5 ml of phosphorus trichloride, the solution is stirred for 2 hours at room temperature, cooled to 0° C. and treated firstly with 50 ml of pyridine and then dropwise at 0°-5° C. with 50 ml of propargyl alcohol. The mixture is stirred for 2 hours at room temperature and then diluted with water. The organic phase is washed successively with water, dilute hydrochloric acid and a 2% aqueous sodium bicarbonate solution, dried over sodium sulphate and evaporated. There is obtained 9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid propargyl ester which melts at 94°-95° C. after absorption on aluminium oxide using benzene as the eluent.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04224244uspto-grants-1980_09