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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508703Generated: November 4, 2026

Chlorotrimethylsilane → Methyl 2-(4-(bromomethyl)phenyl)acetate

https://huagongshe.com/reaction/1508703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant4-(Bromomethyl)phenylacetic acidHCID 4519056—
SolventMethanolHCID 887—
ProductMethyl 2-(4-(bromomethyl)phenyl)acetateHCID 11770640434.3%

Reaction Steps

To a stirred suspension of 2-(4-(bromomethyl)phenyl)acetic acid (5.00 g, 21.8 mmol, 1.0 eq.) in methanol (75 mL) was added chlorotrimethylsilane (0.64 mL, 5.02 mmol, 0.23 eq.) at room temperature. The resulting mixture was stirred at room temperature for 2 hr, at which time the reaction was a clear colorless solution. The volatile material was removed under reduced pressure, the residue dissolved in methanol (25 mL), and the volatile material was removed under reduced pressure. This process was repeated two additional times to afford methyl 2-(4-(bromomethyl)phenyl)acetate as an orange solid (5.30 g, quantitative yield). 1H NMR (CDCl3, 500 MHz) δ 7.37-7.33 (m, 2H), 7.26-7.24 (m, 2H), 4.48 (s, 2H), 3.69 (s, 3H), 3.62 (s, 2H). [Lit. J. Med. Chem. 2009, 52, 1180-9.]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-27bd932e6e2c421493ab07ec9c6c7b08
Source noteuspto-grants-2015_12