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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817513Generated: October 31, 2026

Toluene → Methanefluorodiphosphonate

https://huagongshe.com/reaction/1817513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTributylamineHCID 7622—
ReactantBromotrimethylsilaneHCID 76113—
ReactantTetrapropan-2-yl (fluoromethylene)bis(phosphonate)HCID 12722940—
Solvent1,2-DichloroethaneHCID 11—
SolventDimethylformamideHCID 6228—
ProductMethanefluorodiphosphonateHCID 471181269.5%

Reaction Conditions

Temperature41 °C

Reaction Steps

To a stirred solution of tetraisopropyl fluoromethylenediphosphonate (320 mg, 0.88 mmol) in 1,2-dichloroethane (5 mL) was added dropwise trimethylsilyl bromide (0.70 mL, 5.28 mmol). The resulting solution was stirred at 40-42° C. for 24 h and 3 mL of anhydrous toluene was added. The mixture was concentrated to dryness, and coevaporated with toluene once. The residue was redissolved in DMF (3 mL)/water (2 mL) mixture and concentrated. The residue was mixed with DMF (2 mL) and tributylamine (0.42 mL, 1.76 mmol) and then concentrated to dryness. The residue was coevaporated with anhydrous DMF two times. The resulting residue was dried in a vacuum oven at 30° C. overnight to give a slightly yellow residue (460 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598230B2
Source datasetuspto-grants-2009_10
ORD IDord-001da96a64ec4180911e9d50ff0a49b6
Source noteuspto-grants-2009_10