HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548631Generated: October 30, 2026
1-Methylimidazole → (2-Oxo-1,3-oxazolidin-4-yl)methyl 4-methylbenzene-1-sulfonate
https://huagongshe.com/reaction/548631
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 4-(Hydroxymethyl)-1,3-oxazolidin-2-one | HCID 14456889 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Oxo-1,3-oxazolidin-4-yl)methyl 4-methylbenzene-1-sulfonate | HCID 14456891 | 75% |
Reaction Steps
N-methylimidazole (360 ml, 4.5 mmol, 1.5 eq) is added to a cooled suspension of 4-(hydroxymethyl)-1,3-oxazolidin-2-one a90 (0.35 g, 3 mmol, 1 eq) in dichloromethane (20 ml). p-Toluenesulfonyl chloride a40 (0.63 g, 3.3 mmol, 1.1 eq) in dichloromethane (5 ml) is then added, dropwise. The mixture is stirred at 0° C. for 5 hours then at room temperature for 24 hours. The mixture is then quenched under vigorous stirring with 0.5 ml of water and taken up in chloroform (100 ml). The organic phase is washed with a saturated aqueous solution of sodium hydrogenocarbonate (2×25 ml), with a 1N solution of hydrochloric acid (2×25 ml), with brine, and is dried over magnesium sulfate. The organic layer is concentrated in vacuo to afford 0.61 g of (2-oxo-1,3-oxazolidin-4-yl)methyl 4-methylbenzenesulfonate a91 as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07943605B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-f4ba0346a6fd48c0baec5272191de0e9 |
|---|
| Source note | uspto-grants-2011_05 |
|---|