HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (2R)-1,4-dioxan-2-ylmethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (S)-(1,4-Dioxan-2-yl)methanol | HCID 44429359 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2R)-1,4-dioxan-2-ylmethyl methanesulfonate | HCID 86609782 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
A round bottomed flask was charged with (2S)-1,4-dioxan-2-ylmethanol (115 mg, 0.973 mmol), triethylamine (0.204 mL, 1.46 mmol), and 5 mL of dichloromethane then cooled to −10° C. Methanesulfonyl chloride (91 μL, 1.17 mmol) was added by syringe and the solution was stirred for 30 minutes at −10° C. The solution was diluted in dichloromethane, washed with 1 M HCl, and the aqueous layer was extracted with dichloromethane (2×). The combined organic layers were washed with saturated aquoues sodium bicarbonate (2×) and brine, then dried over sodium sulfate and concentrated to afford (2R)-1,4-dioxan-2-ylmethyl methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893081B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-c18f343f842d47d6bff2ea7b5a867537 |
| Source note | uspto-grants-2011_02 |