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 (86 mg, 0.843 mmol) and triethylamine (136 mg, 1.35 mmol, Shantou Xilong chemical factory) in 10 mL of dichloromethane was stirred at −10° C. for 30 min. Methanesulfonyl chloride (106 mg, 0.927 mmol, Shanghai Haiqu chemical Ltd.) was then added via a syringe. The reaction was stirred at −10° C. for 1 hr at rt and then quenched with 1 mL ice-water. The resulted mixture was extracted with dichloromethane (20 mL×3). The combined organic phases were dried over Na2SO4 and concentrated in vacuo to afford 2-(1-hydroxycyclopropyl)ethyl methanesulfonate as yellow oil (used in the next step without further purification).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426585B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-983862b061ee443fbf3987d51b76e7f3 |
| Source note | uspto-grants-2013_04 |