Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576321Generated: October 30, 2026

Methanol → Methyl 4-(allyloxy)-5-bromo-2-chlorobenzoate

https://huagongshe.com/reaction/576321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant4-(Allyloxy)-5-bromo-2-chlorobenzoic acidHCID 53329405—
ProductMethyl 4-(allyloxy)-5-bromo-2-chlorobenzoateHCID 8671403799%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of compound 21 (17.0 g, 58.0 mmol) in MeOH (380 mL) was added dropwise SOCl2 (21.1 mL, 291 mmol) at 0° C. under an atmosphere of nitrogen. The mixture was stirred at 0° C. for 30 min and then, stirred at 0° C. for 14 hours. The mixture was concentrated in vacuo and poured into aq. saturated NaHCO3 solution and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo to provide the crude product 39 (17.7 g, 99%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034921B2
Source datasetuspto-grants-2015_05
ORD IDord-11d9a7bbf42c4717a84ada1a35044efb
Source noteuspto-grants-2015_05