HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879091Generated: October 31, 2026
Azobisisobutyronitrile → Diethyl 4-(bromomethyl)phenylphosphonate
https://huagongshe.com/reaction/879091
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-Diethoxyphosphoryl-4-methylbenzene | HCID 10868044 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Diethyl 4-(bromomethyl)phenylphosphonate | HCID 12990773 | — |
Reaction Steps
To the suspension of diethyl p-tolylphosphonate (0.73 g, 3.2 mmol) was added a small amount of azobisisobutyronitrile (0.016 g, 0.1 mmol, in portions) and N-bromosuccinimide (0.57 g, 3.2 mmol) in anhydrous CCl4 (30 mL). The mixture was refluxed for 4 h, then cooled to 10° C. and filtered to remove succinimide. The filtrate was washed with water (30 mL) and brine (30 mL) and then dried over anhydrous Na2SO4. After filtration, the crude product was obtained via evaporation of solvent and purified by chromatography on silica gel (hexene/ethyl acetate: 2/1 as eluent) to provide diethyl 4-(bromomethyl)phenylphosphonate as a colorless oil. 1H NMR (500 MHz, CD3Cl): δ 7.79-7.83 (m, 2H), 7.50-7.52 (m, 2H), 4.51 (s, 2H), 4.09-4.18 (m, 4H), 1.33-1.36 (t, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987710B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-39d89588eb9d4d8ba23a3b44cbc12ad6 |
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| Source note | uspto-grants-2015_03 |
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