HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947782Generated: November 3, 2026
Triethyl phosphite → Diethyl 3-Nitrobenzylphosphonate
https://huagongshe.com/reaction/1947782
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | Benzene, 1-(bromomethyl)-3-nitro- | HCID 77568 | — |
| Product | Diethyl 3-Nitrobenzylphosphonate | HCID 13675396 | 98% |
Reaction Steps
A mixture of 3-nitrobenzyl bromide (648 mg, 3.00 mmol) and triethyl phosphite (0.669 mL, 3.90 mmol) was stirred at 140° C. under nitrogen for 16 h. The excess triethyl phosphite was removed under reduced pressure and the residue purified by chromatography over silica gel eluting with 2% MeOH in dichloromethane to afford diethyl(3-nitrobenzyl)phosphonate, 0.80 g (yield: 98%). 1H-NMR (CD3OD, 400 MHz): δ=1.27 (t, J=6.8 Hz, 6H), 3.43 (d, J=22.0 Hz, 2H), 4.08 (q, J=6.8 Hz, 4H), 7.58 (t, J=8.0 Hz, 1H), 7.72 (d, J=7.6 Hz, 1H), 8.15 (d, J=8.4 Hz, 1H), 8.22 (d, J=2.4 Hz, 1H). MS (ES+): m/z 273.99 (MH+). HPLC: tR=2.92 min (ZQ3, polar—5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399433B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-821ee53c5ca64a668864b8d9a29bc753 |
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| Source note | uspto-grants-2013_03 |
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