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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917669Generated: November 1, 2026

Ethyl 7-nitro-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate → HCID 19589924, compound

https://huagongshe.com/reaction/1917669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 7-nitro-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylateHCID 19590114—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 19589924HCID 1958992496.1%

Reaction Steps

According to the procedure described in Example 6A Step 3a mixture of ethyl 7-nitro-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate (1.72 g, 6.8 mmol) and Pd/C (10%, 0.2 g) in EtOAc (100 mL) was stirred under 1 atmosphere of hydrogen at room temperature overnight, to afford ethyl 7-amino-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate as a solid (1.459 g, 96%). 1H NMR (300 MHz, CDCl3) δ 7.41 (s, 1H), 6.18 (s, 1H), 5.41 (br, 2H), 4.30 (m, 4H), 4.19 (q, 2H), 1.38 (t, 3H); LC-MS (ESI) m/z 224 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-6ca8174bfea141f1bae1b16e7ab47658
Source noteuspto-grants-2013_12