HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274603Generated: October 31, 2026
2,5-Dimethoxytetrahydrofuran → HCID 14962883, compound
https://huagongshe.com/reaction/274603
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-Dimethoxytetrahydrofuran | HCID 79098 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Ethyl 4-amino-2-propyl-1H-imidazole-5-carboxylate | HCID 20093493 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 14962883 | HCID 14962883 | — |
Reaction Steps
A solution of ethyl 4-amino-2-propylimidazole-5-carboxylate from above (9.34 g, 47 mmol) and sodium acetate (23.2 g) in acetic acid (100 mL) was heated to reflux and treated with 2,5-dimethoxy-tetrahydrofuran (6.75 mL, 52 mmol). The reaction was held at reflux for 30 minutes, then cooled back to room temperature with an ice bath. The majority of the acetic acid was evaporated under reduced pressure, then the residue was partitioned between ethyl acetate and 10% aqueous K2CO3 (120 mL) each. The organic layer was dried over MgSO4 and evaporated. The residue was purified by flash chromatography on silica gel, eluting with CH2Cl2 -ethyl acetate (80:20). Evaporation of solvents gave a solid which was recrystallized from hexane/EtOAc (1:1) to give 7.4 g of the title compound, mp 134°-135° C.; MS (CI), 248 (m +1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05389661 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-7479a98218bd464a9071c382448dad5c |
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| Source note | uspto-grants-1995_02 |
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