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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956023Generated: November 3, 2026

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

https://huagongshe.com/reaction/1956023

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 11/2 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-methoxyiminoacetamide as a gum (80 mg, 57%). 1H NMR (CDCl3) δ 2.95(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 numberUS05777162
Source datasetuspto-grants-1998_07
ORD IDord-b9e1a004cc534dc8b485e1481662ee71
Source noteuspto-grants-1998_07