HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (Benzyloxy)ethyl 4-bromobenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Benzyloxy) ethanol | HCID 12141 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (Benzyloxy)ethyl 4-bromobenzenesulfonate | HCID 20702450 | 94.3% |
Reaction Steps
A solution of 4-bromobenzenesulfonyl chloride (5.5 g, 21.7 mmol) dissolved in dichloromethane (15 ml) was added dropwise to a solution of 2-benzyloxyethanol (3.0 g, 19.7 mmol) in triethylamine (3 g, 29.6 mmol) at 0° C. under nitrogen. The resultant mixture was stirred for 16 h at room temperature. To the reaction mixture was added water (3 ml) and then the combined mixture was poured onto water (100 ml) and the product was extracted with dichloromethane. The organic layer was washed repeatedly with water and then saturated aqueous sodium hydrogen carbonate solution, before drying (Na2SO4) and concentrating in vacuo to give the title compound as a white solid (6.9 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313312B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-b180f3d65a1b41ecb00e13fb60df5670 |
| Source note | uspto-grants-2001_11 |