Propargyl alcohol → 3-(3,4-Dichlorophenyl)prop-2-yn-1-ol

HRID 1096709

Reaktionsgleichung

[CH2:1]([OH:4])[C:2]#[CH:3].I[C:6]1[CH:11]=[CH:10][C:9]([Cl:12])=[C:8]([Cl:13])[CH:7]=1.C(N(CC)CC)C>C1COCC1.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Cu](I)I>[Cl:12][C:9]1[CH:10]=[C:11]([C:3]#[C:2][CH2:1][OH:4])[CH:6]=[CH:7][C:8]=1[Cl:13]

Komponenten

Reaktionsbedingungen

Temperatur: 35 °C

Versuchsvorschrift

Bis(triphenylphosphine)palladium(II) chloride (120 mg; 0.171 mmol) was added to a stirred solution of propargyl alcohol (5.24 g; 93.4 mmol; 1.02 eq), 1-iodo-3,4-dichlorobenzene (25.0 g; 91.6 mmol, 1 eq), triethylamine (18.5 g; 183.2 mmol, 2 eq), and copper iodide (60 mg; 0.32 mmol) in THF (50 mL). The mixture was stirred at 35° C. for 12 h under a nitrogen atmosphere. The mixture was then filtered through a bed of celite and the filtrate was washed with ethyl acetate. The filtrate was then concentrated at 35° C. (vac.=28 in Hg) using a rotary evaporator. The residue was purified using a silica gel column (4:1 heptane/ethyl acetate→2:1 heptane/ethyl acetate) to give the desired product as a light yellow solid (17.10 g; 85.2 mmol; 93%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 4.53 (s, 2H) 7.19 (d, 1H) 7.29 (d, 1H) 7.49 (s, 1H).

Aufarbeitung

filtrationThe mixture was then filtered through a bed of celite
washthe filtrate was washed with ethyl acetate
concentrationThe filtrate was then concentrated at 35° C. (vac.=28 in Hg)
customa rotary evaporator
customThe residue was purified

Quellen und Nachweise

ORD-Eintrag: ord-5ded2feaa6204fc6b46a0fca13c94c1d
Quelldatensatz: uspto-grants-2012_03
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08138377B2

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