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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991091Generated: October 30, 2026

Aniline → HCID 68533437, compound

https://huagongshe.com/reaction/1991091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTetrahydrofuranHCID 8028—
ReactantStannous ChlorideHCID 24479—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68536085HCID 68536085—
SolventWaterHCID 962—
ProductHCID 68533437HCID 68533437—

Reaction Steps

5.5 g (27.4 mmol) 2-Chloro-1-isobutoxy-4-nitro-benzene was dissolved in 150 ml THF and 30 ml water. After addition of 36.4 g (192 mmol) SnCl2 the reaction mixture was refluxed for 15 minutes. NaHCO3 solution was added, the mixture was extracted with ethyl acetate, dried and concentrated. The crude aniline (5.2 g, 95%) was used without further purification. 2.0 g (10.0 mmol) of the aniline were treated with 1.78 g (10.0 mmol) NBS in 60 ml THF for 20 hours at room temperature. Extraction with ethyl acetate, washings with Na2S2O3 and Na2CO3, drying of the organic phase and removal of solvent yielded 2.75 g of the desired 2-Bromo-5-chloro-4-isobutoxy-aniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645760B2
Source datasetuspto-grants-2010_01
ORD IDord-d2dcc6c171c442b6873aeb2467401822
Source noteuspto-grants-2010_01