반응 #1765

ord-308160af0fe341559cc3cb76dcacfde8

반응 방정식

CCCN(CCC)C1CCc2cc(Br)ccc2C1
6-bromo-2-(N,N-dipropylamino)-1,2,3,4-tetrahydronaphthalene
C=CC(=O)OC
methyl acrylate
Cc1ccccc1P(c1ccccc1C)c1ccccc1C
tri-ortho-tolylphosphine
CCN(CC)CC
triethylamine
CCCN(CCC)C1CCc2cc(/C=C/C(=O)OC)ccc2C1
expected product
수율 28.5%
CCCN(CCC)C1CCc2cc(/C=C/C(=O)OC)ccc2C1
trans-3-[2-(N,N-dipropylamino)-1,2,3,4-tetrahydronaphth-6-yl]prop-2-enoic acid methyl ester
수율 28.5%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture is heated at 125°-130° C. for 3 h 30 min.
  2. 2
    온도cooled
  3. 3
    추출extracted with ethyl acetate
  4. 4
    세척washed with a solution of LiCl

실험 절차

3.1 g (0.01 mol) of 6-bromo-2-(N,N-dipropylamino)-1,2,3,4-tetrahydronaphthalene are dissolved in 50 ml of dimethylformamide. There are added in succession to that solution 0.94 g (0.011 mol) of methyl acrylate, 22.4 mg (0.1 mmol) of palladium acetate, 121 mg (0.4 mmol) of tri-ortho-tolylphosphine and 1.6 ml (0.011 mol) of triethylamine. The mixture is heated at 125°-130° C. for 3 h 30 min. with stirring, cooled, poured into 700 ml of water, extracted with ethyl acetate and washed with a solution of LiCl. After acid to base change, 0.9 g of the expected product is obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05726208uspto-grants-1998_03