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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009139Generated: October 25, 2026

Water → 4-bromo-N-(2-methylbut-3-yn-2-yl)benzenamine

https://huagongshe.com/reaction/1009139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-BromoanilineHCID 7807—
Reactant1-Butyne, 3-chloro-3-methyl-HCID 70679—
CatalystCopperHCID 23978—
CatalystCuprous chlorideHCID 62652—
SolventDiethyl EtherHCID 3283—
Product4-bromo-N-(2-methylbut-3-yn-2-yl)benzenamineHCID 20082271—

Reaction Steps

To a solution of 4-bromobenzenamine (4.0 g, 23 mmol), TEA (4.3 ml, 31 mmol), 2.0 ml of water, copper (0.058 g, 0.91 mmol) and copper(I) chloride (0.058 g, 0.59 mmol) in diethyl ether (9.8 ml, 20 mmol) was added 3-chloro-3-methylbut-1-yne (2.0 g, 20 mmol), dropwise. After stirring overnight, the reaction mixture was transferred to a seperatory funnel containing water and diethyl ether. The aqueous layer was washed 3× with EtOAc. The organic layers were combined, dried with MgSO4, filtered and concentrated. The crude oil was purified with by MPLC (100% DCM to 10% (91/10/1 DCM:MeOH:NH4OH)) to provide the product as an oil. MS m/z: 240 (M+2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973047B2
Source datasetuspto-grants-2011_07
ORD IDord-2df9bcd7cc664ae0af973b6eb19e64f1
Source noteuspto-grants-2011_07