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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3,4-Dihydroxybenzoate | HCID 77547 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate | HCID 16648286 | 23% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09320739B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-08e4457c6f814f9b83d3bebc85b59687 |
|---|
| Source note | uspto-grants-2016_04 |
|---|