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HCID 86702659, compound → HCID 86702658, compound

HRID 2280051
Notes
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Reaction equation

HRID 2280051 reaction equation
[C:1]1(/[CH:7]=[CH:8]/[CH2:9][CH2:10][CH2:11][C:12]#[C:13][C:14](=[O:16])[CH3:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>ClCCCl>[CH2:9]1[C:8]2=[CH:7][C:1]3[C:6]([C:13]([C:14](=[O:16])[CH3:15])=[C:12]2[CH2:11][CH2:10]1)=[CH:5][CH:4]=[CH:3][CH:2]=3
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 86702659HCID 86702659, compound

Product 1

HCID 86702658HCID 86702658, compound

Reagents, catalysts & solvents 1

HCID 111,2-DichloroethaneSolvent

Conditions

Temperature
180 °C

Procedure

To a 0.5-2 mL microwave irradiation vial equipped with a stir bar was added enyne 5a (0.020 g, 0.094 mmol) in DCE (1.6 mL). The reaction was irradiated with stirring at 180° C. for 30 min until complete by TLC. The reaction turned golden in color. The reaction was then transferred to a vial, concentrated under reduced pressure, and dried under vacuum to yield naphthalene 6a as a black oil (0.020 g, quant.).

Workup

  • customTo a 0.5-2 mL microwave irradiation
  • customvial equipped with a stir bar
  • customThe reaction was irradiated
  • concentrationconcentrated under reduced pressure
  • customdried under vacuum
  • Sources & evidence

    ORD record
    ord-15ba7f22b0104297afa6bd7ae1bc2360
    Source dataset
    uspto-grants-2015_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US09133234B2

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes