HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535795Generated: October 29, 2026
Water → 1-((2-Methoxyethoxy)methoxy)-4-((trans)-2-nitrocyclopropyl)benzene
https://huagongshe.com/reaction/535795
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | (E)-1-((2-methoxyethoxy)methoxy)-4-(2-nitrovinyl)benzene | HCID 67064875 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-((2-Methoxyethoxy)methoxy)-4-((trans)-2-nitrocyclopropyl)benzene | HCID 67064876 | 57.6% |
Reaction Steps
Trimethylsulfoxonium iodide (0.76 g, 3.44 mmol) was added in small portions to a suspension of NaH 0.14 g (60% in mineral oil), 3.44 mmol] in dry DMSO (5 mL). The mixture was stirred until gas evolution ceased and a clear solution was formed (45 min). Then, a solution of (E)-1-((2-methoxyethoxy)methoxy)-4-(2-nitrovinyl)benzene (Intermediate J, 0.73 g, 2.86 mmol) in DMSO (5 mL) was transferred via cannula and the reaction was stirred for additional 20 h. The mixture was poured into water (20 mL) and extracted with Et2O (3×15 mL). The organic layers were washed with brine (20 mL), dried over anhydrous Na2SO4 and filtered; after removal of the solvent, the residual orange oil was purified by column chromatography on silica gel (10-20% EtOAc/Hexanes) affording 0.44 g of 1-((2-methoxyethoxy)methoxy)-4-((trans)-2-nitrocyclopropyl)benzene [Rf=0.4 (50% AcOEt/Hexanes), colorless oil, 36% yield].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859555B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-049121c7a1c84912b86cea124df14ac8 |
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| Source note | uspto-grants-2014_10 |
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