HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Methyl 2-(4-acetyl-5-methyl-1H-pyrazol-1-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 2-(4-acetyl-5-methyl-1H-pyrazol-1-yl)acetic acid | HCID 63276965 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-(4-acetyl-5-methyl-1H-pyrazol-1-yl)acetate | HCID 67181907 | 99% |
Reaction Steps
To a solution of 2-(4-acetyl-5-methyl-1H-pyrazol-1-yl)acetic acid (1.17 g, 6.42 mmol, as a mixture of regioisomers from the previous step) in MeOH (8.8 ml)-Toluene (30.6 ml) was added a 2 M solution of (trimethylsilyl)diazomethane in ether (4.8 ml, 9.6 mmol) dropwise at 0° C. The resulting solution was allowed to warm to rt and stirred for 120 min. The reaction was quenched by addition of AcOH (3 ml) and the solvent was concentrated in vacuo. The crude product was purified by silica gel column chromatography (CH2Cl2:MeOH=30:1) to give the desired product along with a mixture of regioisomers (>99% yield). 1H NMR (270 MHz, CDCl3) δ 2.45 (3H, s), 2.53 (3H, s), 3.79 (3H, s), 4.90 (2H, s), 7.88 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07964732B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-482840abe9c74daa8b9da94f887c52c0 |
| Source note | uspto-grants-2011_06 |