Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 23317113 | HCID 23317113 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23317121 | HCID 23317121 | 93.7% |
Reaction Steps
2.31 g of N,N-diethyl 2-(3,4-dichloroanilino)propionamide were dissolved in 15 ml of dry tetrahydrofuran. This solution was added dropwise in 5 minutes to a stirred suspension of 0.61 g of lithium-aluminium-hydride in 25 ml of dry tetrahydrofuran. The reaction mixture was refluxed for 6 hours and was left to stand overnight. The next day 0.6 ml of water, 1.5 ml of 15% sodium hydroxide solution and 1.5 ml of water were added successively. After filtration the organic layer was washed with water, dried and filtered. After evaporating the solvent, 2.06 g of the desired product were obtained; identification by means of thin-layer chromatography. The product was purified by means of columnchromatography (acetone as an eluent), after which 1.41 g of an organge oil was obtained; nD25 =1.5404.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04286983 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-334aed929ffc436cb12fd4519c79fc26 |
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| Source note | uspto-grants-1981_09 |
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