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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzene, 1,3-bis(bromomethyl)-HCID 69373—
ReactantDiethyl methylphosphoniteHCID 85063—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-(bromomethyl)benzyl(methyl)phosphinateHCID 5781677344%

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338593B2
Source datasetuspto-grants-2012_12
ORD IDord-426d1d3b096c45459a79773d33a786f5
Source noteuspto-grants-2012_12