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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17935Generated: October 25, 2026

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

https://huagongshe.com/reaction/17935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantCesium carbonateHCID 10796—
ReactantEthyl 3,4-DihydroxybenzoateHCID 77547—
SolventDimethylformamideHCID 6228—
ProductEthyl 2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylateHCID 1664828629.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of Cs2CO3 (270 g, 1.49 mol) in DMF (1000 mL) were added 3,4-dihydroxybenzoic acid ethyl ester (54.6 g, 0.3 mol) and 1,2-dibromoethane (54.3 g, 0.29 mol) at room temperature. The resulting mixture was stirred at 80° C. overnight and then poured into ice-water. The mixture was extracted with EtOAc (200 mL×3). The combined organic layers were washed with water (200 mL×3) and brine (100 mL), dried over Na2SO4 and concentrated to dryness. The residue was purified by column (Petroleum Ether/Ethyl Acetate 50:1) on silica gel to obtain 2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid ethyl ester (18 g, 29%). 1H NMR (300 MHz, CDCl3) δ 7.53 (dd, J=1.8, 7.2 Hz, 2H), 6.84-6.87 (m, 1H), 4.22-4.34 (m, 6H), 1.35 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741321B2
Source datasetuspto-grants-2010_06
ORD IDord-e552298db658481b8fb18b076fefdd83
Source noteuspto-grants-2010_06