HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → 1-Propanol, 3-(trimethylsilyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Propanol, 3-(trimethylsilyl)- | HCID 76213 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Propanol, 3-(trimethylsilyl)- | HCID 76213 | — |
| Product | Methanesulfonate | HCID 85257 | — |
Reaction Steps
Methanesulfonylchloride (0.73 ml, 9 mmol) was added dropwise to a solution of 3-(trimethylsilyl)-1-propanol (1.2 ml, 7.56 mmol) cooled at 0° C. in 20 ml of dichloromethane. After 45 minutes stirring, the reaction mixture was partitioned between water and dichloromethane, the organic phase was separated, the solvent was evaporated under reduced pressure to afford the expected 3-(trimethylsilyl)-1-propanol, methanesulfonate in crude quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05536732 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-be159df48cbd409fabadf77353b4cf44 |
| Source note | uspto-grants-1996_07 |