HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 23716562, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | Dimethyl 1-eicosanyloxycarbonylphosphonate | HCID 10646503 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23716562 | HCID 23716562 | — |
Reaction Steps
Demethylation of dimethyl 1-eicosanyloxycarbonylphosphonate with NaI was carried out as described in Example 8 above except for the solvent, which was a mixture of DMF (3 mL), THF (8 mL), and acetone (2 mL); yield 0.86 g (84%); mp 95-96° C.; IR (KBr): υ 2960, 2930, 2860, 1735, 1470, 1235, 1220 cm−1; 1H NMR (CDCl3+CD2OD) δ0.8-1.8 (m, 39H, CH3(CH2)18), 3.8 (d, 3H, P(ONa)(OCH3)), 4.2 (t, 2H, CH2O). Anal. Calcd. for C22H44O5NaP: C, 59.69; H, 10.04; N, 5.19; P, 7.00. Found: C, 59.94; H, 10.00; Na, 5.19; P, 7.06.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06686462B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-7a4465518d8042aa94c58ab1d48faed4 |
| Source note | uspto-grants-2004_02 |