HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 4-(Benzyloxy)benzene-1-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-(Benzyloxy)benzenesulfonic acid | HCID 11335143 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Benzyloxy)benzene-1-sulfonyl chloride | HCID 4738385 | 89% |
Reaction Steps
A solution of 55 ml (639 mmol) of oxalyl chloride in 250 ml of dichloromethane is added dropwise to a solution of 61 g (213 mmol) of the sodium salt of 4-benzyloxybenzenesulfonic acid in 200 ml of dimethylformamide, while maintaining the temperature between −20° C. and −10° C. After addition, the reaction medium is slowly brought back to ambient temperature and then stirred for 18 h, poured onto ice and extracted with ethyl acetate. The organic phase is washed with water and with a saturated aqueous solution of sodium chloride and concentrated under vacuum. 54 g (89%) of 4-benzyloxybenzenesulfonyl chloride are obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420632B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-f1c0a3f257e34cdabd173f8b50ab6216 |
| Source note | uspto-grants-2013_04 |