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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906069Generated: October 25, 2026

Acrylamide → N-(4-phenoxybutyl)acrylic amide

https://huagongshe.com/reaction/1906069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylamideHCID 6579—
ReactantPhenothiazineHCID 7108—
ReactantPotassium HydroxideHCID 14797—
Reactant(4-Bromobutoxy)benzeneHCID 70986—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
ProductN-(4-phenoxybutyl)acrylic amideHCID 1365088381.7%

Reaction Steps

Added to 20 ml of N,N-dimethylformamide were 1.34 g of acrylic amide and 3.4 g of (4-bromobutoxy)benzene. With stirring, 0.88 g of flaky potassium hydroxide which had been ground in a mortar was added. Phenothiazine was added in an amount of 0.5% based on the acrylic amide. After they were reacted at 0°-5° C. for 6 hours, insoluble matter was filtered off from the liquid reaction mixture. The solvent and unreacted raw materials were distilled off from the filtrate. The residue was extracted with benzene-water, thereby obtaining the intended product in the benzene layer. Benzene was then driven off from the benzene layer to obtain 2.66 g of N-(4-phenoxybutyl)acrylic amide (yield: 81%). It was purified further with column chromatography in which silica gel and benzene were used as an adsorbent and developer respectively. Its melting point was measured and its elementary analysis was also conducted. The following results were obtained. Melting point: 46°-47° C. Elementary analysis data: C, 71.29% (Calculated: 71.19%); H, 7.31% (7.82%); N, 6.15% (6.38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04649219
Source datasetuspto-grants-1987_03
ORD IDord-71aba9a4503b4bf4900cc95103847716
Source noteuspto-grants-1987_03