HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034563Generated: October 30, 2026
Water → Ethyl 5-methyl-3-(nitromethyl)hexanoate
https://huagongshe.com/reaction/1034563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | HCID 25206188 | HCID 25206188 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl 5-methyl-3-(nitromethyl)hexanoate | HCID 14463328 | 94.8% |
Reaction Steps
10.0 g (34 mmol) of 2-(3-methyl-1-nitromethyl-butyl)-malonic acid diethyl ester (XII, R1=ethyl) were dissolved in 140 mL of DMSO. Water (10.4 mL) and solid NaCl (14.6 g) were added and the mixture was heated for 6 hours at 150° C. After complete conversion, the reaction mixture was cooled to 25° C. and 150 mL of methyl tert-butyl ether were added. 100 mL of water were added slowly. The heterogeneous mixture was stirred for 5 minutes prior to layer separation. The aqueous layer was washed once with 75 mL of methyl tert-butyl ether. The organic layers were combined and washed once with 50 mL of water. The combined organic layers were dried and the volatiles were removed under reduced pressure to give 7.0 g of 5-methyl-3-nitromethyl-hexanoic acid ethyl ester (VIII, R1=ethyl; 93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546112B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-b78177830a1643d3a4238b1c5d1e58e2 |
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| Source note | uspto-grants-2013_10 |
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