HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-(p-Toluenesulfonyl)ethyl 5-chlorosulfonyl-2-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Ethanol, 2-[(4-methylphenyl)sulfonyl]- | HCID 89682 | — |
| Reactant | 5-Chlorosulphonyl-2-anisic acid | HCID 104007 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(p-Toluenesulfonyl)ethyl 5-chlorosulfonyl-2-methoxybenzoate | HCID 22479362 | 81% |
Reaction Steps
A mixture of 5-chlorosulfonyl-2-methoxybenzoic acid (Intermediate 6, 3.0 g, 12.0 mmol) and SOCl2 (6 mL) was heated to reflux temperature for 2 h. Then excess SOCl2 was removed by distillation. The resulting residual oil was dissolved in 20 mL of CH2Cl2 and 2-(p-toluenesulfonyl)ethanol (available from Aldrich 2.0 g, 10 mmol) in 10 mL of CH2Cl2 was added at room temperature. The resulting mixture was heated to reflux temperature for 3 h. Thereafter volatile materials were removed under reduced pressure and the residual oil was purified by column chromatography (silica gel, hexane:CH2C2=1:1 to CH2Cl2) to give 3.5 g (81%) of 2-(p-toluenesulfonyl)ethyl 5-chlorosulfonyl-2-methoxybenzoate (Intermediate 7) as clear thick oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06897227B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-ba40d2f2c684407687619a106ab4e900 |
| Source note | uspto-grants-2005_05 |