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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880591Generated: October 26, 2026

Trimethylsilyldiazomethane → Methyl 4-[2-(2-bromo-5-methoxyphenyl)-1-methylethyl]benzoate

https://huagongshe.com/reaction/1880591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantBenzene methanolHCID 21927730—
Reactant4-[2-(2-Bromo-5-methoxyphenyl)-1-methylethyl]benzoic acidHCID 67485710—
SolventAcetic AcidHCID 176—
ProductMethyl 4-[2-(2-bromo-5-methoxyphenyl)-1-methylethyl]benzoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318760B2
Source datasetuspto-grants-2012_11
ORD IDord-715f8ba8b5f0443aa0c72f6cf5bb63f8
Source noteuspto-grants-2012_11