Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-(2-hydroxyethyl)-beta-alanine | HCID 222905 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Benzene, 1-(chloromethyl)-3(or 4)-ethenyl- | HCID 11768772 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | HCID 53651268 | HCID 53651268 | — |
Reaction Steps
Into the same flask as in Example 1, N-(2-hydroxyethyl)-β-alanine (117 parts), sodium ethylate (68 parts), ethylene glycol (300 parts) and ethylene glycol monomethyl ether (150 parts) are charged, and the resultant mixture is heated at 100° C. under stirring. A mixture of vinylbenzyl chloride (152 parts) and ethylene glycol monomethyl ether (100 parts) is dropwise added thereto in 2 hours. Stirring under heating is further continued for 6 hours. The reaction mixture is neutralized with hydrochloric acid, and acetone is added thereto to precipitate a white solid substance. The white solid substance is collected by filtration and dried under reduced pressure to give N-(2-hydroxyethyl)-N-(vinylbenzyl)-β-alanine (191 parts) of the formula: ##STR21## of which the NMR chart is shown in FIG. 8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04543216 |
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| Source dataset | uspto-grants-1985_09 |
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| ORD ID | ord-4f3db73baccd40bca322e85893ea1826 |
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| Source note | uspto-grants-1985_09 |
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