Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4877Generated: October 23, 2026

Water → Sodium 3,5-di-(2,4-di-tert-amylphenoxypropylcarbamoyl)benzenesulfinate

https://huagongshe.com/en/reaction/4877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BicarbonateHCID 516892—
Reactant3,5-Di-(2,4-di-tert-amylphenoxypropylcarbamoyl)benzenesulfonyl chlorideHCID 86744057—
SolventAcetonitrileHCID 6342—
ProductSodium 3,5-di-(2,4-di-tert-amylphenoxypropylcarbamoyl)benzenesulfinateHCID 6763590382.8%

Reaction Conditions

Temperature30 °C

Reaction Steps

To 2 g (0.016 mol) of sodium sulfite and 2.4 g (0.029 mol) of sodium hydrogen carbonate were added 100 ml of water and 20 ml of acetonitrile and the mixture was stirred at 30° C. To the mixture was added dropwise a solution of 10.5 g (0.013 mol) of 3,5-di-(2,4-di-tert-amylphenoxypropylcarbamoyl)benzenesulfonyl chloride obtained in the aforesaid step dissolved in 100 ml of acetonitrile. After stirring the resultant mixture for one hour, the reaction mixture was poured onto ice water and extracted with 150 ml of ethyl acetate. The ethyl acetate layer was washed thrice with cold water and dried over Glauber's salt. After filtrating away the Glauber's salt, the residue was concentrated to dryness to provide 8.6 g (yield of 82.8%) of a solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05242785
Source datasetuspto-grants-1993_09
ORD IDord-1552f7df163c4dd28c6db945c2a62da2
Source noteuspto-grants-1993_09