HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327035Generated: October 31, 2026
Tetrahydrofuran → HCID 19734465, compound
https://huagongshe.com/reaction/327035
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 148455-50-9 | HCID 4346467 | — |
| Product | HCID 19734465 | HCID 19734465 | — |
Reaction Steps
3.4 g (10 mmol) of 4-(3-chlorophenyl)-3-(ethoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-5-carboxylic acid and 2 g (10 mmol) of carbonyldiimidazole are stirred overnight at room temperature in 50 ml of abs. THF. The mixture is evaporated, the residue is taken up in 50 ml of ethyl acetate and the mixture is washed twice with 50 ml of water each time. After drying over Na2SO4, the solvent is distilled off and the residue (3.55 g) is dissolved in 10 ml of abs. THF. After addition of 100 ml of ethylene glycol and 100 mg of NaH, the mixture is stirred at room temperature for 3 h, mixed with 100 ml of ethyl acetate and extracted twice by shaking with 100 ml of water each time. After drying over sodium sulphate, the extract is evaporated. The residue is homogeneous in the TLC and is further processed directly. Yield: 2.95 g (83% of theory)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05272161 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-b1176af4ff7943d6b9c5610b124bf197 |
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| Source note | uspto-grants-1993_12 |
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