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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991416Generated: November 3, 2026

Water → N-methyl-2-(2-bromomethylphenyl)-2-methoxyiminoacetamide

https://huagongshe.com/reaction/991416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(2-hydroxymethylphenyl)-2-methoxyimino-N-methylacetamideHCID 54472560—
SolventTetrahydrofuranHCID 8028—
ProductN-methyl-2-(2-bromomethylphenyl)-2-methoxyiminoacetamideHCID 5379020457%

Reaction Conditions

Temperature0 °C

Reaction Steps

Carbon tetrabromide (0.33 g) was added to a solution of N-methyl-2-(2-hydroxymethylphenyl)-2-methoxyiminoacetamide (0.11 g) and triphenylphosphine (0.26 g) in tetrahydrofuran (10 ml) at 0° C. The reaction mixture was stirred at 0° C. for 1½ hours and then at room temperature for 1 hour. The reaction mixture was then poured into water and extracted three times with ethyl acetate. The combined extracts were washed with brine and dried over magnesium sulphate. The solution was then concentrated under reduced pressure to leave a gum. Column chromatography (eluting with diethyl ether on silica gel) gave the N-methyl-2-(2-bromomethylphenyl)-2-methoxyimino-acetamide as a gum (80 mg, 57%). 1H NMR (CDCl3) δ2.95(d,3H), 4.0(s,3H), 4.35(s,2H), 6.8(brs,1H), 7.1-7.5(m,4H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465457B1
Source datasetuspto-grants-2002_10
ORD IDord-5e4a6f1e925849f286927a5d7d934790
Source noteuspto-grants-2002_10