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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629785Generated: November 2, 2026

Ammonium Hydroxide → Ethyl 2-amino-2-methyl-4-oxo-4-p-tolylbutanoate

https://huagongshe.com/reaction/1629785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant(E)-Ethyl 2-methyl-4-oxo-4-p-tolylbut-2-enoateHCID 86685877—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-amino-2-methyl-4-oxo-4-p-tolylbutanoateHCID 8668587655.2%

Reaction Steps

To a solution of Intermediate 102A (1.067 g, 4.59 mmol) in DMSO (20 mL) under argon was added NH4OH (18.04 mL, 271 mmol) and the reaction mixture was stirred at rt overnight. The reaction mixture was diluted with EtOAc (75 mL) and washed sequentially with water (40 mL) and brine (20 mL). The organic phase was dried over MgSO4 and concentrated in vacuo to give a yellow oil. The oil was purified by silica gel chromatography (120 g silica gel) to provide the desired product (0.632 g, 55%) as a clear oil. LCMS Anal. Calc'd for C14H19NO3 249.14, found [M+H] 250.1. 1H NMR (500 MHz, CDCl3) δ 7.83 (d, J=8.25 Hz, 2H), 7.24 (d, J=7.98 Hz, 2H), 4.14 (dd, J=7.15, 2.75 Hz, 2H), 3.65 (d, J=17.61 Hz, 1H), 3.20 (d, J=17.61 Hz, 1H), 2.40 (s, 3H), 2.18-2.27 (m, 2H), 1.39 (s, 3H), 1.19 (t, J=7.01 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791091B2
Source datasetuspto-grants-2014_07
ORD IDord-83a9b17334c149558e2297885d4429fc
Source noteuspto-grants-2014_07