HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyldiazomethane → Benzeneacetic acid, 2-(bromomethyl)-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | [2-(Bromomethyl)phenyl]acetic acid | HCID 12889260 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzeneacetic acid, 2-(bromomethyl)-, methyl ester | HCID 15168495 | 32% |
Reaction Steps
To an ice-cold solution of (2-bromomethylphenyl)acetic acid (1 g, 4.4 mmol) in THF (2.4 mL) was added trimethylsilyldiazomethane (3 mL of a 2 M solution in hexanes, 6 mmol), and the reaction mixture was stirred for 14 h. The reaction was quenched with AcOH, and the solvent was removed under reduced pressure. Purification by flash column chromatography (silica, eluent 98:2 to 94:6 methylene chloride/hexanes) afforded methyl (2-bromomethylphenyl)acetate as a light yellow solid (0.34 g, 32%): 1H NMR (300 MHz, CDCl3) δ 7.40-7.20 (m, 4H), 4.59 (s, 2H), 3.81 (s 2H), 3.71 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07629363B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-25ce4c23dd6047b99e4328e5588af330 |
| Source note | uspto-grants-2009_12 |