Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585571Generated: October 27, 2026

Ammonium Chloride → Tert-butyl 5-amino-3,3-dimethyl-5-oxopentanoate

https://huagongshe.com/reaction/585571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
Reactant5-(Tert-butoxy)-3,3-dimethyl-5-oxopentanoic acidHCID 15631255—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 5-amino-3,3-dimethyl-5-oxopentanoateHCID 2192792482%

Reaction Steps

5-Tert-butoxy-3,3-dimethyl-5-oxopentanoic acid (6 g, 27.8 mmol) was dissolved in DMF (111 mL) and benzotriazol-1-yloxytris(pyrrolidino)phosphonium hexafluorophosphate (21.68 g, 41.7 mmol), 1-hydroxybenzotriazole (5.6 g, 41.7 mmol), diisopropylethylamine (19.3 mL, 111 mmol) and ammonium chloride (3 g, 55.6 mmol) were added. The mixture was stirred at room temperature for two hours. The DMF was removed under reduced pressure and the residue dissolved in ethyl acetate. The ethyl acetate was washed with 1N KHSO4, saturated sodium bicarbonate, brine, dried (Na2SO4) and concentrated. The residue was again dissolved in ethyl acetate, washed with 0.1N HCl, 0.1N NaOH, H2O, dried (Na2SO4), passed through a pad of silica and concentrated to give 4.9 g (82%) of the desired product. 1H NMR (DMSO-d6) 7.19 (br s, 1H), 6.71 (br s, 1H), 2.23 (s, 2H), 2.08 (s, 2H), 1.4 (s, 9H), 1.02 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933304B2
Source datasetuspto-grants-2005_08
ORD IDord-e8bca9f807c24725bb001c9ca2d05c4a
Source noteuspto-grants-2005_08