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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-4-iodo-1,1,2,2-tetrafluorobutaneHCID 44717735—
SolventDimethylformamideHCID 6228—
Product2-(4-Bromo-3,3,4,4-tetrafluorobutyl)-malonic acid diethyl esterHCID 5826094274%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889888B2
Source datasetuspto-grants-2014_11
ORD IDord-4ae3c467b7a940c6af365dcd54d8a2c9
Source noteuspto-grants-2014_11