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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881863Generated: October 27, 2026

4-(Tert-butoxy)-4-oxobutanoic acid → (R)-tert-butyl 4-(1-(4-bromophenyl)-4-ethoxy-4-oxobutan-2-ylamino)-4-oxobutanoate

https://huagongshe.com/reaction/881863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Tert-butoxy)-4-oxobutanoic acidHCID 4139107—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(R)-ethyl 3-amino-4-(4-bromophenyl)butanoate hydrochlorideHCID 86648197—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(R)-tert-butyl 4-(1-(4-bromophenyl)-4-ethoxy-4-oxobutan-2-ylamino)-4-oxobutanoateHCID 5960777472.9%

Reaction Steps

To a solution of 4-tert-butoxy-4-oxobutanoic acid (2.38 g, 13.64 mmol) in DMF (30 mL) and DCM (30 mL) is added (R)-ethyl 3-amino-4-(4-bromophenyl)butanoate hydrochloride (4 g, 12.4 mmol), HATU (5.19 g, 13.64 mmol), and TEA (6.91 mL, 49.6 mmol). After stirring at room temperature for 2 hours, the reaction is quenched with H2O, and the crude is diluted with EtOAc, the organic layer is washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give (R)-tert-butyl 4-(1-(4-bromophenyl)-4-ethoxy-4-oxobutan-2-ylamino)-4-oxobutanoate (4.0 g). HPLC retention time=1.70 minutes (condition A); MS (m+1)=444.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993631B2
Source datasetuspto-grants-2015_03
ORD IDord-7302ab906079403898003aad73e4297c
Source noteuspto-grants-2015_03