Formaldehyde → HCID 23044724, 화합물
반응식
[CH2:1]([P:18](=[O:33])([O:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[O:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[P:2](=[O:17])([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[O:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].C=O.[CH2:36](NCC)C>CO>[C:1]([P:2](=[O:17])([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[O:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])([P:18](=[O:33])([O:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[O:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH2:36]참가 물질
5
실험 절차
22.2 g (44.0 mmol) of tetra-n-hexyl 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, about 17 g of tetra-n-hexyl ethenylidenebisphosphonate is produced as a clear liquid.
후처리
- temperatureThis mixture is then refluxed for 48 hours
출처 및 근거
- ORD 기록
- ord-00170c87b5f84ed6a030b4fab7efb88f
- 출처 데이터셋
- uspto-grants-1989_04
- 특허 번호
- US04820698
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