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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351780Generated: October 27, 2026

Sodium Bicarbonate → 5-cyano-N-[2-(4-hydroxy-2-methoxymethoxyphenyl)ethyl]-2-methoxybenzenesulfonamide

https://huagongshe.com/reaction/1351780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-Cyano-2-methoxybenzene-1-sulfonyl chlorideHCID 11528751—
Reactant4-(2-Aminoethyl)-3-methoxymethoxyphenolHCID 17856219—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-cyano-N-[2-(4-hydroxy-2-methoxymethoxyphenyl)ethyl]-2-methoxybenzenesulfonamideHCID 1785628189.4%

Reaction Steps

4-(2-Aminoethyl)-3-methoxymethoxyphenol (12.3 g) and 7.9 g of sodium bicarbonate were suspended in a mixture of 133 mL of tetrahydrofuran and 14.4 mL of water, to the suspension was added 18 mL portions of a solution of 14.50 g of 5-cyano-2-methoxybenzensulfonyl chloride in 180 mL of tetrahydrofuran every 10 minutes while the internal temperature was kept at 10–20° C. After being stirred at room temperature for 8 hours, the reaction mixture was purified by column chromatography on aminopropylated silica gel (eluent: ethyl acetate), and recrystallized from ethyl acetate-diisopropyl ether to give 21.87 g of 5-cyano-N-[2-(4-hydroxy-2-methoxymethoxyphenyl)ethyl]-2-methoxybenzenesulfonamide as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217832B2
Source datasetuspto-grants-2007_05
ORD IDord-7c55c1a700964a25896e2ff5148dc097
Source noteuspto-grants-2007_05