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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425954Generated: October 28, 2026

1-(5-(4-Bromophenyl)-4-hydroxythiophen-3-YL)ethan-1-one → HCID 73224890, compound

https://huagongshe.com/reaction/2425954

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-(4-Bromophenyl)-4-hydroxythiophen-3-YL)ethan-1-oneHCID 44207290—
ReactantHCID 57688120HCID 57688120—
SolventIsopropanolHCID 3776—
ProductHCID 73224890HCID 7322489072%

Reaction Steps

2-(4-Bromophenyl)-3-hydroxy-4-methylcarbonylthiophene (50.1 mg, 0.17 mmol) and 5-hydrazinocarbonylthiophene-2-carboxylic acid (furan-2-ylmethyl)amide (45.0 mg, 0.17 mmol) prepared in Reference Synthetic Example 13 in 2-propanol (4.0 mL) were heated with p-tosylic acid monohydrate (6 mg) at 100° C. for 7.5 hours and cooled to room temperature. The precipitated solid was recovered by filtration, washed with 2-propanol (1 mL) and dried to give the desired product (yield 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968542B2
Source datasetuspto-grants-2011_06
ORD IDord-eddb01e00c264df4b2531801955a230a
Source noteuspto-grants-2011_06