HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437988Generated: November 1, 2026
1,2-Dimethoxyethane → HCID 21427644, compound
https://huagongshe.com/reaction/437988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethyl (2-oxoheptyl)phosphonate | HCID 580181 | — |
| Reactant | HCID 21427641 | HCID 21427641 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21427644 | HCID 21427644 | — |
Reaction Steps
A solution of 1.25 g. of this benzyl alcohol in 75 ml. of chloroform is added to a slurry of 12.5 g. of activated manganese dioxide in 75 ml. of chloroform. The mixture is stirred for one hour, filtered and the solvent is evaporated to leave 2-(6-carbomethoxyhexyl)benzaldehyde as a clear oil. To a slurry of 260 ml. of a dispersion of sodium hydride in mineral oil in 40 ml. of dimethoxyethane is added a solution of 1.31 g. of dimethyl(2-oxoheptyl)phosphonate in 25 ml. of dimethoxyethane. The slurry is stirred for one hour, cooled to 0° C. and 1.22 g. of the benzaldehyde in 20 ml. of dimethoxyethane is added. The mixture is stirred at 0° for 30 minutes and at room temperature for three hours. It is then neutralized with acetic acid and the solvent removed in vacuo. The residue is chromatographed on silica gel to yield 1-(6-carbomethoxyhexyl)-2-(3-oxo-trans-1-octenyl)benzene as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04032656 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-e4565da8a3c448f88c0e5e00cc2c52ff |
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| Source note | uspto-grants-1977_06 |
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