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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554826Generated: October 31, 2026

Water → tert-butyl 4-((1R)-1-aminopropyl)-2-nitrobenzoate

https://huagongshe.com/reaction/554826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactanttert-butyl 4-((1R)-1-aminopropyl)-2-nitrobenzoate D-tartarateHCID 86634888—
SolventEthyl AcetateHCID 8857—
Producttert-butyl 4-((1R)-1-aminopropyl)-2-nitrobenzoateHCID 66934844—

Reaction Steps

Tert-butyl 4-((1R)-1-aminopropyl)-2-nitrobenzoate D-tartarate (15g) was suspended in ethyl acetate (75 ml). Water and a 5N aqueous sodium hydroxide solution were added and the mixture stirred and the layers were separated. The aqueous layer was extracted again with ethyl acetate. The combined organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. Then activated carbon was added to the obtained organic layer and the resultant mixture was stirred for 1 hour. The activated carbon was removed by filtration, and the filtrate was concentrated in vacuo to obtain the title compound (8.9 g) as an oily substance. The 1H-NMR spectral data matched those of Example 322.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049006B2
Source datasetuspto-grants-2011_11
ORD IDord-4fdbfab1d0ec4b8794350efcab378723
Source noteuspto-grants-2011_11