HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025065Generated: October 31, 2026
Trimethylsilyldiazomethane → Methyl 3-(2-(4-fluorophenyl)-3-(methylcarbamoyl)benzofuran-5-yl)benzoate
https://huagongshe.com/reaction/1025065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 3-[2-(4-Fluorophenyl)-3-(methylcarbamoyl)-1-benzofuran-5-yl]benzoic acid | HCID 59275424 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 3-(2-(4-fluorophenyl)-3-(methylcarbamoyl)benzofuran-5-yl)benzoate | HCID 59275138 | 97% |
Reaction Steps
Trimethylsilyldiazomethane (500 μL, 1.00 mmol, 2M in diethyl ether) was added to a stirring solution of 3-(2-(4-fluorophenyl)-3-(methylcarbamoyl)benzofuran-5-yl)benzoic acid (100 mg, 0.257 mmol) in diethyl ether (2.5 mL) at 25° C. It was allowed to stir for 2 hours. The mixture was concentrated to afford the titled compound (100 mg, 97%). LC-MS retention time: 2.46 min; m/z (MH+): 404. LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a Waters SunFire 5 u C18 4.6×50 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 5 ml/min, a gradient of 100% solvent A/0% solvent B to 0% solvent A/100% solvent B, a gradient time of 3 min, a hold time of 1 min, and an analysis time of 4 min where solvent A was 10% acetonitrile/90% H2O/0.1% trifluoroacetic acid and solvent B was 10% H2O/90% acetonitrile/0.1% trifluoroacetic acid. MS data was determined using a Micromass Platform for LC in electrospray mode.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722688B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-45d57cd6ef594deb818eefad9bc2a11d |
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| Source note | uspto-grants-2014_05 |
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