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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69152Generated: October 25, 2026

N-Methoxy-N-methylquinoline-6-carboxamide → 1-(Quinolin-6-yl)ethan-1-one

https://huagongshe.com/reaction/69152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylquinoline-6-carboxamideHCID 55211172—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
SolventTetrahydrofuran tolueneHCID 22635083—
Product1-(Quinolin-6-yl)ethan-1-oneHCID 258559—

Reaction Conditions

Temperature0 °C

Reaction Steps

Methylmagnesium bromide (190 mL of a 1.4 M solution in toluene/THF 3:1, 270 mmol) was added over 35 min to a solution of quinoline-6-carboxylic acid methoxy-methyl-amide (Stage 1.5, 26 g, 120 mmol) in THF at 0° C. under nitrogen. The RM was stirred for 30 min at 0° C. and then allowed to warm up to rt. The RM was quenched with 1 M HCl and the THF removed under reduced pressure. The residue was taken up in EtOAc and the organic layer separated, dried and concentrated to give the title compound as a yellow solid (tR 1.0 min (conditions 1), MH+=172).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-b400a060e54b478684a09a7f1a29c10e
Source noteuspto-grants-2014_09