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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643542Generated: October 25, 2026

Allyl bromide → Methyl 2-allyloxy-5-methoxybenzoate

https://huagongshe.com/reaction/1643542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-hydroxy-5-methoxybenzoateHCID 4072341—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-allyloxy-5-methoxybenzoateHCID 5956045582.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

K2CO3 (4.64 g, 33.6 mmol) and allyl bromide (1.56 mL, 18.5 mmol) were added to a solution of methyl 2-hydroxy-5-methoxybenzoate (2.5 mL, 16.8 mmol) in DMF (10 mL). The reaction mixture was heated to 60° C. for 1 h, and then quenched with H2O (80 mL) and extracted with EtOAc (2×80 mL). The organic layers were washed with H2O (150 mL), dried over MgSO4 and concentrated. The residue was purified by flash column chromatograph eluting with 5-10% EtOAc/hexane to give a colorless oil (3.07 g, 82%). 1H NMR (400 MHz, CDCl3) δ 7.34 (d, J=3.28 Hz, 1 H) 6.98-7.03 (m, 1H) 6.90-6.94 (m, 1 H) 6.01-6.11 (m, 1 H) 5.44-5.51 (m, 1 H) 5.25-5.31 (m, 1 H) 4.57 (td, J=3.28, 1.52 Hz, 2 H) 3.91 (s, 3 H) 3.80 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-bc709be029b4426c946ba915689a8a83
Source noteuspto-grants-2012_02