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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104284Generated: October 30, 2026

N-Methoxy-N-methylacetamide → 1-(3-Bromophenyl)propan-2-one

https://huagongshe.com/reaction/2104284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylacetamideHCID 537505—
ReactantHCID 178419662HCID 178419662—
SolventDiethyl EtherHCID 3283—
Product1-(3-Bromophenyl)propan-2-oneHCID 2734093—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-methoxy-N-methylacetamide (10 g, 0.10 mol) in 200 mL of ether at 0° C. was added 3-bromobenzylmagnesium bromide (0.25 M, 200 mL, 50 mmol). After stirring at 0° C. for 2 h, the reaction mixture was partitioned between hexane and saturated aqueous ammonium chloride. The organic layer was separated, washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to dryness to give the title compound, which was used without further purification. 1H NMR (500 MHz, CD3OD): δ 7.5-7.1 (m, 4H), 3.78 (s, 2H), 2.19 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576239B2
Source datasetuspto-grants-2009_08
ORD IDord-316372ca0ab04197baaf625b4257338c
Source noteuspto-grants-2009_08