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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628447Generated: October 26, 2026

4-Amino-3-hydroxybutanoic acid → Methyl 4-[(2,6-dinitrophenyl)amino]-3-hydroxybutanoate

https://huagongshe.com/reaction/1628447

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3-hydroxybutanoic acidHCID 2149—
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-2,6-dinitrobenzeneHCID 11814—
ReactantThionyl ChlorideHCID 24386—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-[(2,6-dinitrophenyl)amino]-3-hydroxybutanoateHCID 86632868100.7%

Reaction Steps

To a solution of rac-4-amino-3-hydroxybutyric acid (2.00 g, 16.8 mmol) in methanol (40 mL) was added thionyl chloride (1.72 mL, 23.6 mmol) at 0° C. The resultant mixture was stirred at room temperature for 1 hr and concentrated in vacuo. To a mixture of the residue, triethylamine (5.85 mL, 42.0 mmol) and tetrahydrofuran (34 mL) was added 2-chloro-1,3-dinitrobenzene (1.70 g, 8.39 mmol) at room temperature. After the resultant mixture was stirred at 50° C. for 2 hr, the mixture was diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to give the title compound as a yellow solid (2.53 g, 8.45 mmol, quant).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-b3145a0841014183a88aeb0ffa2b3408
Source noteuspto-grants-2014_07