HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 2-(Phenylmethoxy)ethanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-Benzyloxy-ethanesulfonyl chloride | HCID 64179623 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Phenylmethoxy)ethanesulfonamide | HCID 64200908 | — |
Reaction Steps
To a 28% ammonium hydroxide (10 ml) was added dropwise 2-(benzyloxy)ethanesulfonyl chloride (4.1 g) in dichloromethane (10 ml) over 10 minutes under ice-cooling. The mixture was stirred at ambient temperature overnight. The organic layer was separated and the aqueous layer was extracted with dichloromethane/methanol (5/1). The combined organic layer was dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=50/50) to give 2-(benzyloxy)ethanesulfonamide (1.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928264B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-b88c54b646644b2da5bf35f1e027b8dc |
| Source note | uspto-grants-2011_04 |