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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327007Generated: October 30, 2026

Triethylamine → Diisopropyl P-[[(2-(difluoromethoxy)-6-methylphenyl)sulfonyloxy]methyl]phosphonate

https://huagongshe.com/reaction/327007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiisopropyl hydroxymethylphosphonateHCID 10867235—
Reactant2-(Difluoromethoxy)-6-methylbenzene-1-sulfonyl chlorideHCID 18981692—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductDiisopropyl P-[[(2-(difluoromethoxy)-6-methylphenyl)sulfonyloxy]methyl]phosphonateHCID 18981670—

Reaction Steps

A solution of 20 ml of ether, 8.6 g of diisopropyl P-(hydroxymethyl)phosphonate, prepared in Example 17, and 6.9 ml of triethylamine was added dropwise over 25 minutes to 15.2 g of crude 2-methyl-6-(difluoromethoxy)benzenesulfonyl chloride, prepared in Example 3, in 70 ml of ether. After the mild exotherm, the reaction was allowed to stir overnight at room temperature and was then diluted with 200 ml of ethyl acetate, the resulting ethyl acetate solution washed with two 80 ml portions of water, dried with magnesium sulfate, filtered, and concentrated to yield 10.2 g of the very crude desired product as a black oil. The crude product was dissolved in 10 ml of methylene chloride and flash chromatographed on Merck silica gel using ethyl acetate and hexanes. After combining similar fractions, the desired product was isolated as an amber oil in low yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272128
Source datasetuspto-grants-1993_12
ORD IDord-347013a9bcfd4327a908a0f0c94d540e
Source noteuspto-grants-1993_12