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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519288Generated: November 4, 2026

Bromomethyl 4-methoxyphenyl ketone → HCID 86679844, compound

https://huagongshe.com/reaction/1519288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
Reactant2'-Nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl esterHCID 86679832—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86679844HCID 86679844—

Reaction Conditions

Temperature40 °C

Reaction Steps

2-Bromo-4′-methoxyacetophenone (available from Oakwood Products, Inc.; 144.3 mg, 0.63 mmol) was added to a suspension of 2′-nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester (which may be prepared as described for Intermediate 4; 200 mg, 0.63 mmol) in dioxane (4 mL), and the resulting mixture was stirred at 40° C. for 16 h. The precipitate was collected by filtration (187 mg) and used directly in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073881B2
Source datasetuspto-grants-2015_07
ORD IDord-96c73893423b4a9b926d3c10b9555b23
Source noteuspto-grants-2015_07