HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189388Generated: October 30, 2026
Nitrogen → 2-Methanesulfonyloxymethyl-oxazole-4-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1189388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Ethyl 2-(hydroxymethyl)oxazole-4-carboxylate | HCID 10511369 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methanesulfonyloxymethyl-oxazole-4-carboxylic acid ethyl ester | HCID 86664911 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 2-hydroxymethyl-oxazole-4-carboxylic acid ethyl ester (345 mg, 2.02 mmol) in dry CH2Cl2 (10 mL) was treated at 0° C. with Et3N (0.40 mL, 2.87 mmol) followed by DMAP (25 mg, 0.20 mmol) and Ms-Cl (0.20 mL, 2.60 mmol). After stirring at 0° C. for 2 h, the reaction was quenched with water (5 mL). The org. layer was dried over Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (1:2→1:1 EA-Hept) gave the title compound as a yellow solid. TLC: rf (1:1 EA-Hept)=0.23. LC-MS-conditions 01: tR=0.73 min; [M+H]+=249.94.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08674111B2 |
|---|
| Source dataset | uspto-grants-2014_03 |
|---|
| ORD ID | ord-476800d96fe441bbbee46117422a12d4 |
|---|
| Source note | uspto-grants-2014_03 |
|---|