HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915913Generated: October 28, 2026
2-Methoxyethanol → HCID 23024267, compound
https://huagongshe.com/reaction/915913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyethanol | HCID 8019 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methyl 2,4-Dihydroxybenzoate | HCID 16523 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 23024267 | HCID 23024267 | 87.5% |
Reaction Steps
To a 50 ml tetrahydrofuran solution of 4.0 g (23.8 mmol) of methyl 2,4-dihydroxybenzoate, 7.49 g (28.5 mmol) of triphenylphosphine, 2.25 ml (28.5 mmol) of 2-methoxyethanol, and 4.5 ml (28.5 mmol) of diethyl azodicarboxylate were slowly added at 0° C. The mixture was brought to room temperature, and stirred for 1 hour. Then, the reaction mixture was diluted with ethyl acetate, and washed with water and a saturated aqueous solution of sodium chloride. The washed system was dried over sodium sulfate, and then the solvent was distilled off under reduced pressure. To the residue, 100 ml of a solution of ethyl acetate/hexane (=1/4) was added, and insoluble solids were removed by filtration. Then, the mother liquor was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=6/1) to obtain 4.71 g (87%) of the captioned compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07268128B2 |
|---|
| Source dataset | uspto-grants-2007_09 |
|---|
| ORD ID | ord-0e9ead3cf54a4b758161de3ff070449a |
|---|
| Source note | uspto-grants-2007_09 |
|---|