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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373219Generated: October 26, 2026

Dimethylformamide → Tert-butyl[3-(5-benzyloxy-2-nitrophenoxy)benzyl]carbamate

https://huagongshe.com/reaction/1373219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-butyl N-((3-hydroxyphenyl)methyl)carbamateHCID 18369568—
Reactant4-Benzyloxy-2-fluoro-1-nitrobenzeneHCID 22180704—
SolventWaterHCID 962—
ProductTert-butyl[3-(5-benzyloxy-2-nitrophenoxy)benzyl]carbamateHCID 2107310995.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-benzyloxy-2-fluoronitrobenzene (6.43 g, 26 mmols), N-tert-butoxycarbonyl-3-hydroxybenzylamine (5.78 g, 26 mmols), potassium carbonate (3.59 g, 26 mmols) and N,N-dimethylformamide (70 ml) was stirred at 100° C. for 12 hours. The reaction mixture was cooled, then poured into water, and extracted with ethyl acetate. The extract was washed with water, and then dried with anhydrous magnesium sulfate, and the solvent was evaporated away to give an yellow oil of tert-butyl[3-(5-benzyloxy-2-nitrophenoxy)benzyl]carbamate (11.2 g, 95.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160887B1
Source datasetuspto-grants-2007_01
ORD IDord-7c980fa2674f468087cf3b0e4b38d7d5
Source noteuspto-grants-2007_01