HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530167Generated: October 26, 2026
Ethyl oxoacetate → HCID 89775040, compound
https://huagongshe.com/reaction/530167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | (Z)-1-Bromo-4-decene | HCID 10932932 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89775040 | HCID 89775040 | 80.7% |
Reaction Steps
A 100 mL round bottom flask was charged with magnesium turnings (263 mg, 10.9 mmol) and a stirbar. The flask was dried with a heat gun for 5 minutes, cooled under nitrogen before THF (5 mL) and a small grain of iodine was added. A solution of (Z)-1-bromodec-4-ene 3 (2 g, 9.1 mmol) in THF (5 mL) was added slowly. The solution was stirred at room temperature for 2 hours then ethyl glyoxylate (0.375 mL, 1.82 mmol, 50% solution in toluene) was added. Upon completion, the solution was quenched with saturated ammonium chloride solution (5 mL) and stirred until the excess magnesium had dissolved. The solution was diluted with water and extracted with ethyl acetate (3×50 mL). The combined extracts were dried on magnesium sulfate, filtered and concentrated in vacuo to dryness. The residue was purified by column chromatography (100% Hexanes to 20% EtOAc in hexanes) to afford (6Z,16Z)-11-((Z)-dec-4-enyl)docosa-6,16-diene-11,12-diol 29 as a colorless oil (700 mg, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09352042B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-ffcc59b39346495c841fd579f3183f07 |
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| Source note | uspto-grants-2016_05 |
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