Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 2-bromopropionate | HCID 95576 | — |
| Reactant | HCID 14157297 | HCID 14157297 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14157298 | HCID 14157298 | — |
Reaction Steps
To a solution of 3 g of 55% sodium hydride in 70 ml of anhydrous tetrahydrofuran saturated with nitrogen is added dropwise, at room temperature, with stirring and while simultaneously introducing nitrogen, a solution of 16 g N-ethoxyacetyl-2,6-dimethyl-3-nitroaniline in 30 ml of the same solvent. After the weakly exothermic reaction has subsided, the mixture is heated to 55° C. and 12.7 g of methyl 2-bromopropionate in 20 ml of tetrahydrofurane are added. During this addition the temperature rises to 60° C. The mixture is stirred for 12 hours at 55° C., then cooled to room temperature, poured into 100 ml of water and extracted with two 100 ml portions of ethyl acetate. The combined extracts are washed with water, dried over sodium sulfate, and excess solvent is removed in vacuo. The oily crude product is purified by column chromatography over silica gel, using a 1:1 mixture of chloroform/diethyl ether as eluant. Fractions 5 to 30 are combined and the eluant is removed in vacuo. Compound 31 is a viscous oil with a refractive index of nD24 =1.5325.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377587 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-c19dce10b0f04f288bfa016d423da51b |
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| Source note | uspto-grants-1983_03 |
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