HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 21262817, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 21262815 | HCID 21262815 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21262817 | HCID 21262817 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a 0° C. solution of alcohol (535 mg, 1.14 mmol) from step 2 and i-Pr2NEt (436 mL, 2.5 mmol) in 10 mL of anhydrous toluene, was slowly added SOCl2 (145 mnL, 2.0 mmol). The resulting yellow solution was stirred 30 minutes at 0° C., 10 minutes at room temperature, quenched with water and diluted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4 and concentrated under reduced pressure. The residue was used directly for the next step without any purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06180650B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-93f3a2912b6346efbf04f2f85c261ad9 |
| Source note | uspto-grants-2001_01 |