2-Methyl-3-butyn-2-ol → HCID 54574602, Verbindung

HRID 1080563Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1080563
[CH2:1]([C:4]1[CH:9]=[C:8]([F:10])[C:7](I)=[C:6]([F:12])[CH:5]=1)[CH2:2][CH3:3].[CH3:13][C:14]([OH:18])([C:16]#[CH:17])[CH3:15].[I-]>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[Cu].C(N(CC)CC)C>[CH2:1]([C:4]1[CH:9]=[C:8]([F:10])[C:7]([C:17]#[C:16][C:14]([CH3:15])([OH:18])[CH3:13])=[C:6]([F:12])[CH:5]=1)[CH2:2][CH3:3]

Komponenten

7

Versuchsvorschrift

A mixture of 2 g of 1-propyl-3,5-difluoro-4-iodobenzene, 0.626 g of 2-methyl-3-butyn-2-ol, 0.164 g of tetrakis(triphenylphosphine)palladium(0), 10 ml of triethylamine and 0.054 g of copper(l) iodide was stirred at 90° for 2 hours. Then, the cooled reaction mixture was partitioned between water and ether, the ether phase was washed several times with water, dried over magnesium sulphate, filtered over Celite and evaporated on a rotary evaporator. The residue was then chromatographed on 75 g of silica gel (eluent: 10% ethyl acetate in hexane) and again evaporated. There were obtained 1.5 g of 4-(4-propyl-2,6-difluorophenyl)-2-methylbutyn-2-ol as a yellow liquid.

Aufarbeitung

  1. customThen, the cooled reaction mixture
  2. customwas partitioned between water and ether
  3. washthe ether phase was washed several times with water
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered over Celite
  6. customevaporated on a rotary evaporator
  7. customThe residue was then chromatographed on 75 g of silica gel (eluent: 10% ethyl acetate in hexane)
  8. customagain evaporated

Quellen und Nachweise

ORD-Eintrag
ord-d532522f2c61438ca3d08df64a9b43ce
Quelldatensatz
uspto-grants-1996_12
Patentnummer
US05582767

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