Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Diisopropylethylamine | HCID 81531 | — |
Reaction Steps
The compound of formula (XIV) is reacted with a chlorinating agent, such as thionyl chloride, phosphorus oxychloride, and the like, optionally with a base, such as pyridine, and the like, in an organic solvent, such as toluene, benzene, chloroform, methylene chloride, and the like, in a temperature range of 0° C. to 80° C., preferably in the range of 25° C. to 60° C., to yield the corresponding compound of formula (XV). Alternatively, compound of formula (XV) is reacted with a chlorinating agent, such as mesyl chloride, and the like, with a base, such as triethylamine, diisopropylethylamine, and the like, in an organic solvent, such as THF, dichloromethane, chloroform, and the like, in a temperature range of 0° C. to 60° C., preferably in the range of 25° C. to 40° C., to yield the corresponding compound of formula (XV).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076358B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-44f15d13f1b64931ae0c847c08bddf6f |
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| Source note | uspto-grants-2011_12 |
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