HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-(4-Chloro-2-methoxyphenyl)naphthalene-2-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium 5-(4-chloro-2-methoxyphenyl)naphthalene-2-sulfonate | HCID 86687359 | — |
| Product | 5-(4-Chloro-2-methoxyphenyl)naphthalene-2-sulfonyl chloride | HCID 86687361 | 89.2% |
Reaction Steps
A round bottom flask was charged with sodium 5-(4-chloro-2-methoxyphenyl)naphthalene-2-sulfonate (0.137 g, 0.369 mmol) and a septum was attached and the flask flushed with N2. DMF (1.232 mL) was added followed by thionyl chloride (0.081 mL, 1.108 mmol) by syringe at rt, an exotherm was observed. The solution was maintained at rt for 1 h, and then poured into a separatory funnel containing ice. The resulting mixture was extracted with DCM (2×15 mL). The combined organic layers were washed with water (2×10 mL) and brine (1×10 mL) and dried over Na2SO4 and concentrated to give 5-(4-chloro-2-methoxyphenyl)naphthalene-2-sulfonyl chloride (0.121 g, 0.329 mmol), which was used immediately without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012443B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-ed8e263e38784056a24f2134f36fa0c4 |
| Source note | uspto-grants-2015_04 |