HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → 2-(Phenylsulfonyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium benzenesulfonate | HCID 517327 | — |
| Product | 2-(Phenylsulfonyl)ethanol | HCID 30202 | 28.1% |
Reaction Steps
1,000 ml of an aqueous solution containing 509 g (2.16 mol) of sodium benzenesulfonate (dihydrate) was heated to 80°-90° C. and stirred. To this solution were added at the same time 539 g (4.31 mol) of ethylenebromohydrin and 100 ml of an aqueous solution containing 45 g of sodium hydroxide while maintaining the pH of the reaction solution at 7-8. After the addition was completed, the reaction solution was further stirred for 2 hours at 80°-90° C. and then cooled to room temperature. Then, the reaction solution was extracted with ethyl acetate. The ethyl acetate was concentrated and distilled off under reduced pressure to yield 113 g of the desired product having a boiling point of 172 to 174° C./0.4 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USH0000691 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-26aded66af2b4aee8e3157ca3b82bbb1 |
| Source note | uspto-grants-1989_10 |