HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397221Generated: October 31, 2026
Chloromethyl ethyl ether → HCID 12529074, compound
https://huagongshe.com/reaction/2397221
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloromethyl ethyl ether | HCID 18523 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate | HCID 282663 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12529074 | HCID 12529074 | — |
Reaction Steps
In 5 ml. of anhydrous tetrahydrofuran was suspended 193 mg. of a 50% oil dispersion of sodium hydride and after adding to the mixture 7 ml of anhydrous tetrahydrofuran solution of 1 g. of diethyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate, the resultant mixture was stirred at room temperature for a while. The red-brown reaction product thus obtained was cooled to temperatures of from -40° C. to -50° C. and after adding thereto 5 ml. of anhydrous tetrahydrofuran solution of 380 mg. of ethoxymethyl chloride at the same temperature, the mixture was stirred for one hour and 45 minutes at the same temperature. By treating further the reaction product as in Example 1, 370 mg. of white crystals of diethyl 1-ethoxymethyl-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate melting at 125° C. was obtained. The product was confirmed in the infrared absorption spectra and the nuclear magnetic resonance spectra to completely coincide with the presumed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04021434 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-a66fa8e568764ee29d4fba272be8c224 |
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| Source note | uspto-grants-1977_05 |
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