HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Sodium p-benzyloxybenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium P-phenolsulfonate dihydrate | HCID 23666329 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Sodium p-benzyloxybenzenesulfonate | HCID 23685655 | — |
Reaction Steps
Aqueous NaOH (40 mL of a 15% aqueous solution, 150 mmol) is added to 20 g (86.2 mmol) of 4-hydroxybenzenesulfonic acid sodium salt dihydrate at RT. An additional 20 mL of water is added, and the mixture is warmed slightly to dissolve the salt. Benzyl bromide (19.2 g, 112.1 mmol) in 8 mL of ethanol is then added in several portions. The mixture is heated to reflux. After 30 min, additional 20 mL of water is added, and heating is continued for 3.5 h, followed by continued stirring at RT overnight. After cooling in the refrigerator for 3 h, the solid product is collected by filtration and washed with water (20 mL), ethanol (40 mL), and ether (40 mL) and then dried overnight under vacuum to give 4-benzyloxybenzenesulfonic acid sodium salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700637B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-4b52d9ded8864a6e8d5ddd66214fd7d5 |
| Source note | uspto-grants-2010_04 |