HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931353Generated: October 31, 2026
Methyl 5-methyl-3-oxohexanoate → Methyl 5-methyl-2-nitro-3-oxohexanoate
https://huagongshe.com/reaction/931353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 5-methyl-3-oxohexanoate | HCID 121701 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 5-methyl-2-nitro-3-oxohexanoate | HCID 42609287 | — |
Reaction Steps
A solution of sodium nitrite (232 g, 3.36 mol) in water (560 mL) was added drop-wise over 1.5 hours to a solution of methyl 5-methyl-3-oxohexanoate (400 g, 2.53 mol) in glacial acetic acid (510 mL) at 20 to 25° C. Stirring was continued at room temperature for 2 hours. Water (1.3 L) was added, and the reaction mixture was stirred for an additional 18 hours. The mixture was then extracted with ethyl acetate (3×2.5 L), and the combined organic layers were washed sequentially with water (2.5 L), with aqueous sodium bicarbonate solution (2.5 L), and with saturated aqueous sodium chloride solution (1.0 L). After drying over sodium sulfate, the organic extracts were concentrated in vacuo to afford the product as a yellow liquid, which was used directly in the next step. Yield: 456 g, 2.24 mol, 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296761B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-9d2e5ba3772c4588a8501e7003267432 |
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| Source note | uspto-grants-2016_03 |
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