HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Cyclopentylmethanesulfonyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium cyclopentylmethanesulfonate | HCID 23670187 | — |
| Product | Cyclopentylmethanesulfonyl Chloride | HCID 2735404 | — |
Reaction Steps
The subtitle compound was prepared by the method of Preparation 58 from sodium cyclopentylmethanesulfonate [Preparation 64] and thionyl chloride, to afford cyclopentylmethanesulfonyl chloride as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06610707B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-866d82d2a03c41c98c19c15a2187fd5a |
| Source note | uspto-grants-2003_08 |