Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105497Generated: November 2, 2026

Taurine → 2-({2-Hydroxy-3-[(prop-2-en-1-yl)oxy]propyl}amino)ethane-1-sulfonic acid

https://huagongshe.com/reaction/1105497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTaurineHCID 1123—
ReactantAllyl glycidyl etherHCID 7838—
ReactantGlycol monoethyl etherHCID 8076—
ReactantSodium HydroxideHCID 14798—
Catalyst4-NitrosophenolHCID 7729—
SolventWaterHCID 962—
Product2-({2-Hydroxy-3-[(prop-2-en-1-yl)oxy]propyl}amino)ethane-1-sulfonic acidHCID 2215788340.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

Into a 2 liter volume flask equipped with a stirrer, taurine (125 g), sodium hydroxide (40 g), deionized water (200 g) and ethylene glycol monoethyl ether (600 g) were charged. The contents were maintained at 60° C. while stirring, and a mixture of allyl glycidyl ether (114 g) and p-nitrosophenol (0.1 g) was dropwise added thereto in 20 minutes. Thereafter, stirring was continued for 2 hours. The reaction mixture of pH 9 was treated with an ionic exchange resin (Amberlite IR-120) to eliminate Na+ ion, whereby a solution of pH 4 was obtained. The solution was concentrated in a rotary evaporator to make a 7/10 volume so that needle crystals were precipitated. These crystals were identified to unreacted taurine by NMR and IR. The filtrate was poured into a 3 time volume of acetone to precipitate brown oily materials. The oily materials were collected and dried in vacuo as give N-(2-hydroxy-3-allyloxypropyl)taurine (96 g) of the formula: ##STR7##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04309327
Source datasetuspto-grants-1982_01
ORD IDord-15fa9d8b4f7e4b179c3454555725b902
Source noteuspto-grants-1982_01