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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Taurine | HCID 1123 | — |
| Reactant | Allyl glycidyl ether | HCID 7838 | — |
| Reactant | Glycol monoethyl ether | HCID 8076 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | 4-Nitrosophenol | HCID 7729 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-({2-Hydroxy-3-[(prop-2-en-1-yl)oxy]propyl}amino)ethane-1-sulfonic acid | HCID 22157883 | 40.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04309327 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-15fa9d8b4f7e4b179c3454555725b902 |
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| Source note | uspto-grants-1982_01 |
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