HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Trifluoromethanesulfonylamino-butyryl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Trifluoromethanesulfonylamino-butyric acid methyl ester | HCID 86601182 | — |
| Catalyst | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Trifluoromethanesulfonylamino-butyryl chloride | HCID 21886133 | — |
Reaction Steps
4-Trifluoromethanesulfonylamino-butyric acid methyl ester (0.42 g, 1.77 mmol) [example 212, step a] was taken up in methanol [2 mL] and 1N NaOH was added [2.66 mL] and stirred for 2 hours. 1N HCl was added and the product was extracted with ethyl acetate, dried with magnesium sulfate and evaporated. The crude product (0.13 g, 0.57 mmol) was dissolved in dichloromethane/DMF [1 mL/1 drop] and thionyl chloride (0.08 mL, 1.14 was added. The reaction was stirred at room temperature for 2 hours and then evaporated and used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109354B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-e573fb40a0fa4892bf12d366646aedc7 |
| Source note | uspto-grants-2006_09 |