Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407263Generated: October 26, 2026

Sulfuric Acid → Tert-butyl 2-(2,3-difluoro-6-nitrophenyl)-3-oxobutanoate

https://huagongshe.com/reaction/407263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium ChlorideHCID 5234—
ReactantTert-butyl acetoacetateHCID 15538—
Reactant1,2,3-Trifluoro-4-nitrobenzeneHCID 69871—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium 2-methylbutan-2-olateHCID 2733478—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductTert-butyl 2-(2,3-difluoro-6-nitrophenyl)-3-oxobutanoateHCID 44828787—

Reaction Conditions

Temperature70 °C

Reaction Steps

tert-Butyl acetoacetate (3.852 g) was added to a stirred mixture of sodium tert-pentoxide (2.804 g) in toluene (26 ml) at 40° C. The mixture was heated to 70° C. and 1,2,3-trifluoro-4-nitrobenzene (2.00 g) added. The mixture was maintained at 70° C. for 3 hours. The mixture was cooled to 25° C. and 20% w/w sulphuric acid added to adjust the mixture to pH 1. Sodium bicarbonate was added to bring the mixture to pH 5. Water (5 ml) and saturated sodium chloride (5 ml) was added. The lower aqueous layer was discarded and the organic layer is washed successively with water (7 ml), water (7 ml), 2.3% w/w aqueous sodium bicarbonate solution (2.75 ml) and then water (6 ml). The organic layer was distilled under reduced pressure (50 mbar), to leave a solution of tert-butyl 2-(2,3-difluoro-6-nitrophenyl)-3-oxobutanoate in toluene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754240B2
Source datasetuspto-grants-2014_06
ORD IDord-b9c3bfd0e16c4c7abe7c3b2299b58a9f
Source noteuspto-grants-2014_06