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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646125Generated: October 30, 2026

2-(4-Bromophenoxy)-2-methyl-1-(pyrrolidin-1-yl)propan-1-one → 1-(2-(4-Bromophenoxy)-2-methylpropyl)pyrrolidine

https://huagongshe.com/reaction/646125

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Bromophenoxy)-2-methyl-1-(pyrrolidin-1-yl)propan-1-oneHCID 68694781—
SolventTetrahydrofuranHCID 8028—
Product1-(2-(4-Bromophenoxy)-2-methylpropyl)pyrrolidineHCID 6869668676%

Reaction Steps

BH3×THF (1M, 27.0 mmol, 27.0 mL) was added dropwise under argon to 2-(4-bromophenoxy)-2-methyl-1-(pyrrolidin-1-yl)propan-1-one (2.12 g, 6.8 mmol; see step (a)) in THF (40 mL) at 0° C. The reaction was quenched by careful addition of NH4Cl (aq. sat.). The reaction mixture was acidified by HCl (1M). NaOH (aq. 0.5M, 30 mL) was added to the filtrate which was then extracted with CH2Cl2. The combined extracts were washed with brine, dried (Na2SO4), concentrated and distilled under reduced pressure to yield the title compound (1.5 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705023B2
Source datasetuspto-grants-2010_04
ORD IDord-93d0b71ad2134347ac60b247fbac09b3
Source noteuspto-grants-2010_04