HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020880Generated: November 1, 2026
Methyl 4-nitrobutyrate → HCID 57518510, compound
https://huagongshe.com/reaction/1020880
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-nitrobutyrate | HCID 25604 | — |
| Reactant | 2,5-Difluorobenzaldehyde | HCID 137663 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57518510 | HCID 57518510 | — |
Reaction Steps
To a solution of 2,5-difluorobenzaldehyde (3.82 mL, 35.2 mmol) in ethanol (70 mL) was added methyl 4-nitrobutyrate (4.51 mL, 35.2 mmol) and the mixture was stirred for 5 minutes. To the reaction mixture was added ammonium acetate (5.42 g, 70.4 mmol) and the mixture stirred for 10 minutes at ambient temperature and then heated at reflux temperature for 16 h. The solvent was removed in vacuo and to the yellow oil was added saturated aqueous sodium hydrogen carbonate (100 mL) and the aqueous phase extracted with ethyl acetate (3×50 mL). The combined organic phases were washed with saturated aqueous brine (1×50 mL), dried with anhydrous sodium sulfate, filtered and the solvent removed in vacuo. The yellow racemic product was purified by preparative HPLC on a Berger SFC using ChiralPak AS-H™ column, eluting with 20% MeOH/CO2 to give (5R,6S)-6-(2,5-difluorophenyl)-5-nitropiperidin-2-one [LC/MS 257.1 (M+1)] as the second eluting isomer and the title compound as the first eluting isomer. LC/MS 257.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716482B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-af0d94972a7a435e9f137c1ffa3c2ade |
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| Source note | uspto-grants-2014_05 |
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