Formaldehyde → HCID 23044696, Verbindung

HRID 2165343Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2165343
[CH2:1]([P:16](=[O:29])([O:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[O:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[P:2](=[O:15])([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[O:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].C=O.[CH2:32](NCC)C>CO>[C:1]([P:2](=[O:15])([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[O:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])([P:16](=[O:29])([O:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[O:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[CH2:32]

Komponenten

5

Versuchsvorschrift

20.20 g (44.0 mmol) of tetra-n-pentyl methylenebisphosphonate, 6.61 g (220.0 mmol) of paraformaldehyde and 3.22 g (64.0 mmol) of diethylamine are combined with the same reactants and the same conditions as described above in Example I. This mixture is then refluxed for 48 hours. After the methanol is eliminated as described above in Example I. 14.08 g of tetra-n-pentyl ethenylidenebisphosphonate is produced as a clear liquid.

Aufarbeitung

  1. temperatureThis mixture is then refluxed for 48 hours

Quellen und Nachweise

ORD-Eintrag
ord-eb5074bb2b5b4193879fb9d2659d27d5
Quelldatensatz
uspto-grants-1990_07
Patentnummer
US04939284

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