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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395032Generated: October 29, 2026

3-Hydroxyacetanilide → HCID 725681, compound

https://huagongshe.com/reaction/2395032

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxyacetanilideHCID 12124—
ReactantN-[3-(prop-2-en-1-yloxy)phenyl]acetamideHCID 258024—
Reactant1-(Chloromethyl)-3-(2-propen-1-yloxy)benzeneHCID 14169367—
SolventDiphenyl EtherHCID 7583—
SolventHexaneHCID 8058—
ProductHCID 725681HCID 725681—

Reaction Steps

A mixture of N-(3-allyloxyphenyl)acetamide (13.2 g) prepared by a similar method to that of Example 2, Footnote c (A), from N-(3-hydroxyphenyl)acetamide, in Ph2O (100 ml) was heated at 250° C. for 10 minutes, cooled and diluted with hexane (100 ml) to give crystals. The crystals were re-crystallised from ethyl acetate. The liquors were evaporated and dissolved in 0.2M aqueous NaOH, filtered though Celite, and acidified with 1M aqueous HCl solution to give N-(4-allyl-3- hydroxyphenyl)acetamide (3.6 g) mpt. 164°-165° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811459
Source datasetuspto-grants-1998_09
ORD IDord-79c6bde1473548689f8d46caafbc8181
Source noteuspto-grants-1998_09