Triethylamine → HCID 86659759, compound

HRID 45269Notes

Reaction equation

HRID 45269 reaction equation
[C:1]([O:11][CH2:12][CH3:13])(=[O:10])/[CH:2]=[CH:3]/[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6].CCN(CC)CC.Br[C:22]1[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=1>CN(C=O)C.CCOC(C)=O.CC([O-])=O.CC([O-])=O.[Pd+2]>[N:24]1[CH:25]=[CH:26][CH:27]=[C:22](/[C:3](/[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6])=[CH:2]\[C:1]([O:11][CH2:12][CH3:13])=[O:10])[CH:23]=1

Participants

7

Reactant 3

HCID 8471TriethylamineHCID 122863-BromopyridineHCID 6375762-Pentenedioic acid, 1,5-diethyl ester

Product 1

HCID 86659759HCID 86659759, compoundYield 87.1%

Reagents, catalysts & solvents 3

HCID 167845palladium(II) acetateCatalystHCID 6228DimethylformamideSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
40 °C

Procedure

To a solution of 15 mL (85.6 mmol) of diethyl (2E)-pent-2-enedioate in 5 mL of anhydrous DMF are added, under a stream of argon, 0.62 g (2.8 mmol) of Pd(OAc)2, 1.7 g (5.56 mmol) of P(OTol)3 and 5.5 mL (39.7 mmol) of Et3N, the medium is then heated to 40° C. and 4 mL (39.75 mmol) of 3-bromopyridine are added. The medium is then heated for 24 hours at 90° C., and then taken up in 100 mL of EtOAc, washed with 100 mL of water, dried over Na2SO4, concentrated under reduced pressure and purified by chromatography on a column of silica gel, eluting with a cyclohexane/EtOAc gradient of 0 to 10% EtOAc. 9.12 g of diethyl (2Z)-3-(pyridin-3-yl)pent-2-enedioate are obtained in the form of a yellow wax.

Workup

  1. temperatureThe medium is then heated for 24 hours at 90° C.
  2. washwashed with 100 mL of water
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated under reduced pressure
  5. custompurified by chromatography on a column of silica gel
  6. washeluting with a cyclohexane/EtOAc gradient of 0 to 10% EtOAc

Sources & evidence

ORD record
ord-94dd0bfd2b924bf8bf081bc3af40bd4b
Source dataset
uspto-grants-2013_09
Patent number
US08541455B2

Reaction notes

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