HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1-Methanesulfonyloxy-2-allylcyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(Prop-2-en-1-yl)cyclohexan-1-ol | HCID 11789291 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Methanesulfonyloxy-2-allylcyclohexane | HCID 20498897 | — |
Reaction Steps
To a mixture of 250 ml. of dichloromethane, 25 g. 2-allylcyclohexanol and 16.7 g. of triethylamine cooled in an ice-salt bath to -10° C. is added dropwise, over 15 minutes, 18.9 g. of methanesulfonyl chloride. The mixture is cooled at -10° C. to -15° C. for 30 minutes and then washed with 300 ml. each of cold water, 10% hydrochloric acid, sodium carbonate solution and with saturated sodium chloride solution. The organic layer is dried with magnesium sulfate and concentrated in vacuo to give a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04259352 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-79adca8ca5ed4c6e96fea4c8719e822b |
| Source note | uspto-grants-1981_03 |