Formaldehyde → 1-Diethylamino-5-methyl-6-(m-methoxyphenyl)hex-2-yne

HRID 1414943Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1414943
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:9][CH:10]([CH3:14])[CH2:11][C:12]#[CH:13])[CH:6]=[CH:7][CH:8]=1.O1[CH2:20][CH2:19]COO1.C=O.[CH2:23]([NH:25][CH2:26]C)[CH3:24].[OH-].[Na+]>O1CCOCC1.C(O)(=O)C>[CH2:23]([N:25]([CH2:19][CH3:20])[CH2:26][C:13]#[C:12][CH2:11][CH:10]([CH3:14])[CH2:9][C:5]1[CH:6]=[CH:7][CH:8]=[C:3]([O:2][CH3:1])[CH:4]=1)[CH3:24]

Komponenten

8

Versuchsvorschrift

Heat 5-(m-methoxyphenyl)-4-methyl-pent-1-yne (8 g), trioxan (0.5 g), 30% formalin (5.5 cc), diethylamine (4 g), acetic acid (2.75 g), dioxan (25 cc) and cuprous chloride (0.12 g) together at 70° for 15 hours. Make cooled solution alkaline with 10% aqueous sodium hydroxide and extract with ether. Wash the ethereal solution with water and extract with 10% hydrochloric acid (3 × 20 cc). Combine the acid extracts, wash with ether and make alkaline with 10% aqueous sodium hydroxide and extract with ether. Wash the ethereal solution, dry, remove the solvent and distil the residue at 0.1 mm to obtain 1-diethylamino-5-methyl-6-(m-methoxyphenyl)-hex-2-yne.

Aufarbeitung

  1. extractionextract with ether
  2. washWash the ethereal solution with water
  3. extractionextract with 10% hydrochloric acid (3 × 20 cc)
  4. washCombine the acid extracts, wash with ether
  5. extractionextract with ether
  6. washWash the ethereal solution
  7. customdry
  8. customremove the solvent
  9. customdistil the residue at 0.1 mm

Quellen und Nachweise

ORD-Eintrag
ord-37a4af2118a14b51b721f9d68bac3a39
Quelldatensatz
uspto-grants-1977_01
Patentnummer
US04002746

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