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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915464Generated: October 31, 2026

Water → 4-Tert-butyl-3-fluoroaniline

https://huagongshe.com/reaction/1915464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant1-Tert-butyl-2-fluoro-4-nitrobenzeneHCID 59394945—
SolventMethanolHCID 887—
Product4-Tert-butyl-3-fluoroanilineHCID 2190475874%

Reaction Steps

NaBH4 (144 mg, 152 μL, 3.8 mmol) was added to a solution of 1-tert-butyl-2-fluoro-4-nitro-benzene (750 mg, 3.8 mmol) and NiCl2.6H2O (2.6 g, 11 mmol) in methanol (15 mL) at −15° C. After addition, the mixture was stirred for 2 minutes and water was added to quench the reaction. The reaction mixture was extracted with ethyl acetate (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated in vacuo to afford 4-tert-butyl-3-fluoro-aniline (470 mg, 74%) which was used without further purification. 1H NMR (300 MHz, CDCl3) δ 7.08-7.02 (m, 1H), 6.42-6.34 (m, 2H), 1.32 (s, 9H). MS (ESI) m/z: 168.2 [M+H]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614327B2
Source datasetuspto-grants-2013_12
ORD IDord-d2e21e8804784645914206038c313c44
Source noteuspto-grants-2013_12