HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Mercaptoethanol → Ethanol, 2-[[(4-ethenylphenyl)methyl]thio]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | p-Vinylbenzyl chloride | HCID 74126 | — |
| Catalyst | 4-Methoxyphenol | HCID 9015 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethanol, 2-[[(4-ethenylphenyl)methyl]thio]- | HCID 14692798 | 47.9% |
Reaction Steps
A polymerization inhibitor, p-methoxyphenol (1.24 g; 0.01 mole), was added to a mixture of 152 g (1.0 mole) of p-(chloromethyl)styrene, 60 g (1.5 moles) of sodium hydroxide and 0.5 liter of tetrahydrofuran. The resulting mixture was boiled, and 78 g (1.0 mole) of 2-mercaptoethanol was added dropwise over 0.5 hour. The boiling was continued for 3 hours. After cooling to room temperature, the reaction mixture was filtered by the same operation as in Example 1, and distilled under reduced pressure (140-145 ° C./1-2 mmHg) to give 93 g of 2-(4-vinylbenzylthio)ethanol as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05034492 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-bec347d5a4bb4994b6538c4da0066876 |
| Source note | uspto-grants-1991_07 |