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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938413Generated: October 30, 2026

Water → 2-bromo-N-(2-methyl-2-propenyl)-5-nitroaniline

https://huagongshe.com/reaction/1938413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-5-nitroanilineHCID 82607—
Reactant3-Bromo-2-methyl-1-propeneHCID 357785—
SolventTetrahydrofuranHCID 8028—
Product2-bromo-N-(2-methyl-2-propenyl)-5-nitroanilineHCID 2343354832.1%

Reaction Steps

To a suspension of NaH 60% dispersion in oil (97 mg, 0.0023 mol) in 2 mL of anhydrous THF at 0° C. was added 2-bromo-5-nitroaniline (500 mg, 0.0023 mol) in 2 mL of THF dropwise, the temperature was raised to rt to complete deprotonation then lowered to 0° C. 3-bromo-2-methylpropene (232 mL, 0.0023 mol) was added very slowly and the reaction mixture was stirred at 0° C. for 3 h then neutralized with water (5 mL). The mixture was extracted with ethyl acetate (2×10 mL), dried (Na2SO4) and concentrated in vacuo to an oil that was subjected to flash column chromatography (silica gel, hexanes/ethyl acetate, 8:2) to give 200 mg (32%) of 2-bromo-N-(2-methyl-2-propenyl)-5-nitroaniline (structure 55A of Scheme XLVII, where R1 =methyl, R2 =H). Data for 2-bromo-N-(2-methyl-2-propenyl)-5-nitroaniline: 1H NMR (400 MHz, CDCl3) 7.55 (d, J=8.5, 1H), 7.40 (dd, J=8.5, 2.8, 1H), 7.39 (d, J=2.8, 1H), 4.96 (s, 2H), 4.95 (bs, 1H), 3.82 (d, J=5.9, 2H), 1.81 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693646
Source datasetuspto-grants-1997_12
ORD IDord-140a9702d69a47e4a72c16266979b774
Source noteuspto-grants-1997_12