HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197476Generated: October 27, 2026
Water → Ethyl 3-(bromomethyl)benzyl(methyl)phosphinate
https://huagongshe.com/reaction/2197476
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Benzene, 1,3-bis(bromomethyl)- | HCID 69373 | — |
| Reactant | Diethyl methylphosphonite | HCID 85063 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-(bromomethyl)benzyl(methyl)phosphinate | HCID 57816773 | 44% |
Reaction Steps
To a solution of α,α′-Bisbromo-m-xylene (7.75 g, 29.38 mmol) in DMF (10 mL) was added diethyl methylphosphonite (2.0 g, 14.69 mmol) via syringe. The mixture was heated to 150° C. for 2 minutes in a microwave. The reaction mixture was poured into water and product extracted with ethyl acetate (3×25 mL). The combined organics were washed with water (2×50 mL) and brine (50 mL), and dried over Na2SO4. Reduced volume in vacuo and purified product by flash column eluting 20-100% ethyl acetate in hexanes to give 1.89 g mg (44%) 65 as a colorless oil. 1H NMR (300 MHz, CDCl3) δ 1.24 (t, 3H), 1.33 (d, 3H), 3.08 (d, 2H), 3.97 (dt, 2H), 4.44 (s, 2H), 7.25 (m, 4H). LCMS: m/z for C11H16BrO2P++H observed 291.0 and 293.0 at 2.09 minutes of a 3.5 minute run, gradient 5-95% CH3CN in H2O.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338593B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-426d1d3b096c45459a79773d33a786f5 |
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| Source note | uspto-grants-2012_12 |
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