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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49392Generated: October 26, 2026

Acetamide → Benzyl-{2-[4-(2-methyl-oxazol-4-yl)-phenoxy]-ethyl]-carbamate

https://huagongshe.com/reaction/49392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamideHCID 178—
ReactantBenzyl-[2-(4-bromoacetylphenoxy)-ethyl]-carbamateHCID 12986050—
ProductBenzyl-{2-[4-(2-methyl-oxazol-4-yl)-phenoxy]-ethyl]-carbamateHCID 2058795158%

Reaction Conditions

Temperature130 °C

Reaction Steps

Acetamide (2.95 g, 50.0 mmol) and benzyl-[2-(4-bromoacetylphenoxy)-ethyl]-carbamate (1.20 g, 3.06 mmol) were combined in a round-bottomed flask and heated to about 130° C. for about ninety minutes. The reaction mixture was then allowed to cool to room temperature, and the resulting orange solid was partitioned between ethyl acetate and water and extracted three times with ethyl acetate. The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting crude solid was purified by column chromatography (silica gel; methylene chloride to 10% ethyl acetate/methylene chloride) to afford 621 mg (58% yield) of the product as a white solid. LRMS ([M+H]+)=353.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706743B2
Source datasetuspto-grants-2004_03
ORD IDord-8dfdc29225db4d1a972001c5c77782a5
Source noteuspto-grants-2004_03