HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyldiazomethane → Methyl 4-[2-(2-bromo-5-methoxyphenyl)-1-methylethyl]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | Benzene methanol | HCID 21927730 | — |
| Reactant | 4-[2-(2-Bromo-5-methoxyphenyl)-1-methylethyl]benzoic acid | HCID 67485710 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 4-[2-(2-bromo-5-methoxyphenyl)-1-methylethyl]benzoate | HCID 59756903 | — |
Reaction Steps
(Trimethylsilyl)diazomethane (2.0M hexanes, 4.8 mL) was added dropwise to a benzene/MeOH solution (7/3, 50 mL) containing the intermediate from Step A (2.8 g, 8.0 mmol). After 20 minutes AcOH was added dropwise to quench the excess reagent. The solution was concentrated and the residue purified by silica gel chromatography using a hexanes/ethyl acetate gradient to give the title compound. 1H NMR (500 MHz, CDCl3): δ 7.98 (d, J=8.2 Hz, 2H); 7.43 (d, J=8.2 Hz, 1H); 7.29 (d, J=8.2 Hz, 2H); 6.63 (dd, J=3.0, 8.7 Hz, 1H); 6.50 (d, J=3.0 Hz, 1H); 3.93 (s, 3H); 3.68 (s, 3H); 3.26-3.19 (m, 1H); 2.96 (d, J=7.0 Hz, 2H); 1.34 (d, J=6.9 Hz, 3H). LCMS1 4.14 min. (M-31)=331
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318760B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-715f8ba8b5f0443aa0c72f6cf5bb63f8 |
| Source note | uspto-grants-2012_11 |