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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481890Generated: October 31, 2026

Water → N-[(1,1-Dimethylethoxy)carbonyl]-3-[(2-nitrophenyl)amino]-L-alanine

https://huagongshe.com/reaction/1481890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantSodium BicarbonateHCID 516892—
ReactantBoc-Dap-OHHCID 2755946—
SolventDimethylformamideHCID 6228—
ProductN-[(1,1-Dimethylethoxy)carbonyl]-3-[(2-nitrophenyl)amino]-L-alanineHCID 2288194763%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (S)-3-amino-2-tert-butoxycarbonylamino-propionic acid (Aldrich) (5 g, 24.48 mmol) in DMF (75 mL) was added 1-fluoro-2-nitro-benzene (2.92 mL, 26.93 mmol) and sodium bicarbonate (6.17 g, 73.44 mmol) at RT and the resulting mixture was heated at 80° C. for 18 h under nitrogen atmosphere. Water was added and the aqueous layer was washed with ethyl acetate. The pH of the aqueous solution was adjusted to 3 with the addition of 10% aqueous sodium bisulfate solution and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried (Na2SO4) and concentrated under reduced pressure to give crude mass which was triturated with hexanes to afford (S)-2-tert-butoxycarbonylamino-3-(2-nitro-phenylamino)-propionic acid (5 g, 63%) as an orange yellow solid. LC-MS: 326.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409888B2
Source datasetuspto-grants-2016_08
ORD IDord-1f92dc62a6f743649448964b64aaf13f
Source noteuspto-grants-2016_08