HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360534Generated: November 4, 2026
1-Butanol → Methacrylic acid 1-(n-butoxycarbonyl)-1,1-difluoro-2-butyl ester
https://huagongshe.com/reaction/2360534
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methacrylic acid 1-chlorocarbonyl-1,1-difluoro-2-butyl ester | HCID 58352381 | — |
| Product | Methacrylic acid 1-(n-butoxycarbonyl)-1,1-difluoro-2-butyl ester | HCID 86663489 | 91.1% |
Reaction Steps
Into a 1 L glass flask with a dropping funnel, 62.8 g (0.847 mol, 1.2 eq) of n-butanol, 510 g of diisopropyl ether, 100 g (0.988 mol, 1.4 eq) of triethylamine and 1 g of antioxidant “Nonflex MBP” (manufactured by Seiko Chemical Co., Ltd.) were added. The resulting solution was cooled to 0° C. and stirred, followed by dropping thereto 170 g (purity: 99%, 0.706 mol) of methacrylic acid 1-chlorocarbonyl-1,1-difluoro-2-butyl ester. The thus-obtained reaction solution was stirred for 1 hour at room temperature. The completion of the reaction was confirmed by 19F NMR. The reaction-completed solution was separated into an organic layer and an aqueous layer by the addition of 500 mL of water. The organic layer was dehydrated with magnesium sulfate, filtrated, and then, concentrated under a reduced pressure. The concentration residue was subjected to distillation under a reduced pressure. With this, 179 g of methacrylic acid 1-(n-butoxycarbonyl)-1,1-difluoro-2-butyl ester was obtained as a colorless transparent liquid (yield: 91%, purity: 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686098B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-61770f73d3f64fcdbd3f75849c83f717 |
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| Source note | uspto-grants-2014_04 |
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