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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793210Generated: November 3, 2026

Sodium Bicarbonate → 1-(5-Hydroxy-6,7-dimethyl-benzofuran-2-yl)-2-morpholin-4-yl-ethanone

https://huagongshe.com/reaction/1793210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantAcetic acid 6,7-dimethyl-2-(2-morpholin-4-yl-acetyl)-benzofuran-5-yl esterHCID 10236780—
SolventMethanolHCID 887—
Product1-(5-Hydroxy-6,7-dimethyl-benzofuran-2-yl)-2-morpholin-4-yl-ethanoneHCID 1023641054.8%

Reaction Steps

A solution of acetic acid 6,7-dimethyl-2-(2-morpholin-4-yl-acetyl)-benzofuran-5-yl ester (23 mg), prepared as in Example 17, in MeOH (10 mL) was stirred while sodium bicarbonate (10 mg) was added. Then the mixture was stirred at RT overnight, followed by evaporation to dryness. The residue was purified by silica gel column, eluting with 5% MeOH in dichloromethane to give 11 mg of 1-(5-hydroxy-6,7-dimethyl-benzofuran-2-yl)-2-morpholin-4-yl-ethanone as an oil. Conversion into HCl salt gave a yellow solid. 1H NMR (CD3OD, 300 MHz) δ:: 7.60 (s, 1H), 7.20 (s, 1H), 3.78(m, 6H), 2.64(m, 4H), 2.50(s, 3H), 2.40(s, 3H) ppm. 13C NMR (CDCl3, 75 MHz)δ: 187.98, 170.20, 153.31, 152.29, 146.58, 130.44, 124.53, 122.80, 114.36, 113.15, 64.69, 53.79, 21.28, 13.47, 12.86 ppm. M/S 290 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078541B2
Source datasetuspto-grants-2006_07
ORD IDord-4b842ae5328c45729c573b6344de6cb9
Source noteuspto-grants-2006_07