HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895513Generated: October 28, 2026
Sulfuric Acid → Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate
https://huagongshe.com/reaction/1895513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | ethyl 2,2-difluorohexanoate | HCID 10464909 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate | HCID 11118722 | 44.1% |
Reaction Steps
A solution of dimethyl methylphosphonoate (6.5 g, 80 mmol, 2.2 equiv) in tetrahydrofuran (100 mL) was cooled to −78° C. and n-butyllithium (2.5 M in hexanes, 14 mL, 36 mmol, 1 equiv) was added dropwise. The solution was stirred at −78° C. for 30 min and ethyl 2,2-difluorohexanoate (6.5 g, 36 mmol, 1 equiv) was added dropwise. The solution was stirred at −78° C. for 1 h and warmed to 0° C. over 1 h. Pentane (100 mL) was added followed by the dropwise addition of 2M H2SO4 to pH=6. The aqueous layer was separated and extracted with pentane (3×15 mL). The organics were combined, dried over sodium sulfate, filtered, and concentrated to dryness under vacuum on a rotary evaporator. The crude oil was purified by column chromatography using methyl tert-butyl ether as eluant to afford 4.1 g of 26 as a yellow oil (44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513441B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-41241caa9de44b518b03358f17f51363 |
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| Source note | uspto-grants-2013_08 |
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