HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338820Generated: October 30, 2026
Hydrochloric Acid → 2-(4-Bromo-3,3,4,4-tetrafluorobutyl)-malonic acid diethyl ester
https://huagongshe.com/reaction/338820
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-4-iodo-1,1,2,2-tetrafluorobutane | HCID 44717735 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Bromo-3,3,4,4-tetrafluorobutyl)-malonic acid diethyl ester | HCID 58260942 | 74% |
Reaction Steps
In nitrogen atmosphere, 1900 mL of dimethylformamide was prepared with the addition of 320 g (7.17 mol) of sodium hydride (60% mineral oil-containing product), followed by putting it in an iced bath with the addition of 1208 g (7.17 mol) of diethyl malonate. After 1 hour of stirring, 2400 g (7.17 mol) of 1-bromo-1,1,2,2-tetrafluoro-4-iodobutane was added to this solution while regulating the reaction solution so as to be not higher than 100° C. After 1 hour of stirring, 1000 mL of 1N hydrochloric acid was added thereto, followed by extracting it with diisopropyl ether. Then, an organic layer was concentrated, followed by distillation under reduced pressure (115-116° C./0.53 kPa), thereby obtaining 1940 g of the objective 2-(4-bromo-3,3,4,4-tetrafluorobutyl)-malonic acid diethyl ester (74% yield, 89% GC purity) in the form of a light yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889888B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-4ae3c467b7a940c6af365dcd54d8a2c9 |
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| Source note | uspto-grants-2014_11 |
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