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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327004Generated: October 26, 2026

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

https://huagongshe.com/reaction/327004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiisopropyl hydroxymethylphosphonateHCID 10867235—
Reactant2-Chloro-6-methylbenzene-1-sulfonyl chlorideHCID 15725370—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductDiisopropyl P-[[(2-chloro-6-methylphenyl)sulfonyloxy]methyl]phosphonateHCID 1898163691.6%

Reaction Steps

A solution of 21.7 g of 2-chloro-6-methylbenzenesulfonyl chloride dissolved in 40 ml of ether was added dropwise over 90 minutes to a mixture of 20.6 g of diisopropyl P-(hydroxymethyl)-phosphonate, (Example 17), 80 ml of ether, and 15.4 ml of triethylamine. The addition was mildly exothermic and the reaction was cooled using a cool water bath (no ice). The reaction was allowed to stir overnight at room temperature and then was diluted with 300 ml of ethyl acetate, washed with three 100 ml portions of water, the organic phase dried with magnesium sulfate, filtered and concentrated under reduced pressure to yield 34.0 g of the desired product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272128
Source datasetuspto-grants-1993_12
ORD IDord-105c062a50c448c68aa14775b0f6893f
Source noteuspto-grants-1993_12