HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892623Generated: November 1, 2026
Phosphorus oxychloride → HCID 69272498, compound
https://huagongshe.com/reaction/1892623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Oxalic acid dihydrate | HCID 61373 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18117857 | HCID 18117857 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69272498 | HCID 69272498 | 84% |
Reaction Steps
Phosphorus oxychloride (119.372 g, 778.83 mmol) was added to a stirred solution of N-(2-benzo[1,3]dioxol-5-yl-ethyl)-2-(4-bromophenyl)acetamide 35 (9.400 g, 25.951 mmol) in anhydrous acetonitrile (225 mL) and refluxed for 6 h. The reaction mixture was concentrated under reduced pressure, methanol was added to it, and again concentrated the solvent under reduced pressure. The obtained residue was dissolved in methanol, to this solution was added sodium borohydride (17.700 g, 467.118 mmol) and the mixture was stirred overnight at room temperature. The solvent was removed under reduced pressure, the residue was dissolved in CHCl3, washed with 1N NaOH solution, water and dried over Na2SO4. The organic layer was evaporated under reduced pressure and the oily mass was dissolved in CHCl3. A solution of oxalicacid dihydrate (6.543 g, 51.902 mmol) in methanol was added to above solution with stirring at room temperature followed by addition of ether. The mixture was stirred for 2 h at the same temperature and kept in the refrigerator overnight. Filtered the solid and washed with ether, and air dried to afford 37 as white solid (9.5 g, 84%). 1H NMR (300 MHz, DMSO-d6) δ 7.55 (d, J=7.5 Hz, 2H, ArH), 7.31 (d, J=7.8 Hz, 2H, ArH), 6.79 (s, 1H, ArH), 6.73 (s, 1H, ArH), 5.99 (s, 2H, CH2), 4.63 (t, J=6.3 Hz, 1H, —CH), 3.36-3.32 (m, 2H, CH2), 3.18-3.06 (m, 2H, CH2), 2.96-2.82 (m, 2H, —CH2). MS (ES+) m/z 346 [M-(COOH)2+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507523B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-48187822928041a18aa10a90b6232945 |
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| Source note | uspto-grants-2013_08 |
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