HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 14692797, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ar-Vinylbenzyl chloride | HCID 170249 | — |
| Catalyst | 4-Methoxyphenol | HCID 9015 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14692797 | HCID 14692797 | 54% |
Reaction Steps
A polymerization inhibitor, p-methoxyphenol (1.24 g; 0.01 mole), was added to a mixture of 78 g (1.0 mole) of 2-mercaptoethanol, 133 g (1.0 mole) of a 30 % aqueous solution of sodium hydroxide and 0.15 liter of methanol. While the mixture was cooled to below 10° C., 152 g (1.0 mole) of m-(chloromethyl)styrene was added dropwise over 3 hours. Then, the reaction mixture was continuously stirred for an additional 3 hours to complete the reaction. Water (1 liter) was added to the reaction mixture to separate it into an oil layer and an aqueous layer. The oil layer was washed with water and distilled under reduced pressure (140°-150 ° C./1-2 mmHg) to give 105 g of 2-(3-vinylbenzylthio)ethanol as a colorless transparent liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05034492 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-40af544f80cd4d1b91b8f6a6b9a4782a |
| Source note | uspto-grants-1991_07 |