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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613374Generated: October 30, 2026

Water → tert-Butyl 4-[N-(tert-Butoxycarbonyl)-N-(methoxycarbonyl)aminomethyl]-3-nitrobenzoate

https://huagongshe.com/reaction/613374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantt-Butyl 4-bromomethyl-3-nitrobenzoateHCID 18462578—
ReactantPotassium t-butyl methyl iminodicarboxylateHCID 86754983—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-[N-(tert-Butoxycarbonyl)-N-(methoxycarbonyl)aminomethyl]-3-nitrobenzoateHCID 1959194973%

Reaction Steps

To a solution of tert-butyl 4-bromomethyl-3-nitrobenzoate (2.27 g, 7.2 mmol) (Int. J. Peptide Res. 1990, 36, 31) in dimethylformamide (25 mL) was added a suspension of potassium tert-butyl methyl iminodicarboxylate (J.C.S. Perkin I 1977, 1088-90) (1.56 g, 7.3 mmol) in dimethylformamide (20 mL). The dark brown solution was stirred 1 h and poured into water (400 mL), extracted with ethyl acetate (3×100 mL) and the combined organic layers were washed with water (5×75 mL), dried (sodium sulfate) and concentrated to give a pale orange oil which was purified by flash chromatography on silica gel (20% ethyl acetate/hexane) to give the title compound (2.15 g, 73%): 1H NMR (400 MHz, CDCl3) δ 8.65 (s, 1H), 8.2 (d, 1H), 7.45 (d, 1H), 5.3 (s, 2H), 3.8 (s, 3H), 1.6 (s, 9H), 1.45 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008213
Source datasetuspto-grants-1999_12
ORD IDord-5b8472431fa6446eb478c2e491917903
Source noteuspto-grants-1999_12