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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327002Generated: October 29, 2026

Triethylamine → HCID 15405454, compound

https://huagongshe.com/reaction/327002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
ReactantDiethyl phosphonomethanolHCID 76513—
Reactant2-Chloro-6-methylbenzene-1-sulfonyl chlorideHCID 15725370—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductHCID 15405454HCID 1540545487.2%

Reaction Steps

A solution of 4.63 g of 2-chloro-6-methylbenzenesulfonyl chloride dissolved in 20 ml of anhydrous ether was added dropwise over a 15 minute period to a mixture of 3.50 g of diethyl P-(hydroxymethyl)phosphonate (Example 17), 5 ml of triethylamine and 15 ml of anhydrous ether. The addition was mildly exothermic and a white precipitate began to form shortly after the addition of the sulfonyl chloride was begun. The reaction was stirred at room temperature overnight. After 48 hours of additional stirring the reaction solution was diluted with 200 ml of ethyl acetate and 80 ml of water. The organic phase was washed with two 90 ml portions of water, dried with magnesium sulfate, filtered and concentrated to yield 6.4 g of an oil which solidified upon standing, mp 41°-43° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272128
Source datasetuspto-grants-1993_12
ORD IDord-0d01e251672f4789a72338a3ae6116cf
Source noteuspto-grants-1993_12