HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632240Generated: November 1, 2026
Diethyl Ether → Dimethyl (2-oxohept-5-yn-1-yl)phosphonate
https://huagongshe.com/reaction/1632240
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl (2-oxohept-5-yn-1-yl)phosphonate | HCID 13269871 | — |
Reaction Steps
To a solution of 3.2 g of dimethyl methanephosphonate in 52 ml of tetrahydrofuran was added at -78° C. 155 ml of n-butyl lithium (1.59N) and the mixture was stirred for 25 mins at -78° C. To the mixture was added at -78° C. a solution of 1.6 g of the above-mentioned ester in 3.2 ml of tetrahydrofuran. The mixture was stirred for 15 mins and for one hour at room temperature. After addition of 100 ml of ether to the reaction mixture, the mixture was washed with 30 ml of aqueous saturated solution of oxalic acid, 50 ml of water and 40 ml of aqueous saturated solution of sodium chloride. The washed mixture was dried and concentrated to give an oily material. The oily material was distilled under reduced pressure to yield 2.2 g of dimethyl 2-oxo-hept-5-yne-phosphonate (143° to 146° C./0.7 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04474802 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-e146ff3869ee4237a5e25089f99bfffe |
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| Source note | uspto-grants-1984_10 |
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