HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-2-methoxybenzene-1-sulfonyl chloride → N-(5-bromo-2-hydroxymethyl-phenyl)-5-chloro-2-methoxybenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-2-methoxybenzene-1-sulfonyl chloride | HCID 2734272 | — |
| Reactant | (2-Amino-4-bromophenyl)methanol | HCID 53440895 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(5-bromo-2-hydroxymethyl-phenyl)-5-chloro-2-methoxybenzenesulfonamide | HCID 66789377 | 82% |
Reaction Steps
A solution of (2-amino-4-bromo-phenyl)-methanol (1.53 g, 7.57 mmol) in pyridine (15 mL) was treated with 5-chloro-2-methoxybenzenesulfonyl chloride (1.85 g, 7.57 mmol) at room temperature and stirred for 72 h, then poured upon ice-cold 2 M aq. hydrochloric acid solution and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4), and evaporated to produce a gummy residue, from which the product was precipitated by addition of toluene. The precipitate was collected by filtration and dried to afford N-(5-bromo-2-hydroxymethyl-phenyl)-5-chloro-2-methoxy-benzenesulfonamide (2.51 g, 82%). Off-white solid, MS (ISP)=404.2 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030308B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-8ecfda0949a747b7897e65f00a34f470 |
| Source note | uspto-grants-2011_10 |