HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(1-Hydroxycyclopropyl)ethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-(2-Hydroxyethyl)cyclopropan-1-ol | HCID 13306871 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1-Hydroxycyclopropyl)ethyl methanesulfonate | HCID 86640792 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
A mixture of 1-(2-hydroxyethyl)cyclopropanol (310 mg, 3.04 mmol) and triethylamine (614.1 mg, 6.08 mmol) in 10 mL of dichloromethane was stirred at −10° C. for 30 min. Methanesulfonyl chloride (348 mg, 3.04 mmol) was added via a syringe. After stirring at −10° C. for 1 hr, the reaction mixture was quenched with ice-water (2 mL) and extracted with dichloromethane (20 mL×4). The combined organic phases were dried over Na2SO4 and concentrated in vacuo to give yellow oil (used for the next step quickly).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232294B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-1b71481da4df4d14be75da6cb994ad10 |
| Source note | uspto-grants-2012_07 |