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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631222Generated: October 30, 2026

1,2-Dibromoethane → Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate

https://huagongshe.com/reaction/631222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3,4-DihydroxybenzoateHCID 77547—
SolventDimethylformamideHCID 6228—
ProductEthyl 2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylateHCID 1664828623%

Reaction Conditions

Temperature70 °C

Reaction Steps

According to the procedure described in Example 6A Step 1, a mixture of ethyl 3,4-dihydroxybenzoate (5.465 g, 30 mmol), 1,2-dibromoethane (5.636 g, 30 mmol), and K2CO3 (6.219 g, 45 mmol) in DMF (100 mL) was heated at 70° C. overnight. The residue was purified by silica gel chromatography with 20-50% EtOAc/hexane as eluants to afford ethyl 2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate as an oil (1.423 g, 23%). 1H NMR (300 MHz, CDCl3) δ 7.58 (d, 1H), 7.56 (dd, 1H), 6.88 (d, 1H), 4.30 (m, 6H), 1.37 (t, 3H); LC-MS (ESI) m/z 209 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09320739B2
Source datasetuspto-grants-2016_04
ORD IDord-08e4457c6f814f9b83d3bebc85b59687
Source noteuspto-grants-2016_04