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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206694Generated: November 2, 2026

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

https://huagongshe.com/reaction/2206694

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 numberUS09371303B2
Source datasetuspto-grants-2016_06
ORD IDord-cd42639a16ae4904a72be7bf3b771da0
Source noteuspto-grants-2016_06