HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1,4-Bis(6-chloropyridin-3-yl)butane-1,4-diyl dimethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1,4-Bis(6-chloropyridin-3-yl)butane-1,4-diol | HCID 59617171 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,4-Bis(6-chloropyridin-3-yl)butane-1,4-diyl dimethanesulfonate | HCID 59616994 | 99.9% |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
The product from Example 207B (2.23 g, 7.12 mmol) and triethylamine (2.98 mL, 21.36 mmol) were combined in dichloromethane (50 mL). The mixture was cooled to −20° C. and methanesulfonyl chloride (1.383 mL, 17.80 mmol) was added. The mixture was stirred at room temperature for 1 hour. The solvent was evaporated to give the title product (approx 3.34 g) which was directly used for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691938B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-04c6c3a4e929494b9bd18d0202a209bb |
| Source note | uspto-grants-2014_04 |