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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606584Generated: October 27, 2026

Formaldehyde → Ethyl 3-methyl-5-(4-methyl-morpholin-2-ylmethoxy)-benzofuran-2-carboxylate

https://huagongshe.com/reaction/606584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactantethyl 3-methyl-5-(4-Boc-morpholin-2-ylmethoxy)-benzofuran-2-carboxylateHCID 67046655—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 3-methyl-5-(4-methyl-morpholin-2-ylmethoxy)-benzofuran-2-carboxylateHCID 67046419—

Reaction Steps

Ethyl 3-methyl-5-(4-Boc-morpholin-2-ylmethoxy)-benzofuran-2-carboxylate (1.05 mmol) was dissolved in 30 ml of a 4.0 M solution of hydrochloric acid in dioxan and stirred at room temperature for 1 hour. After removing the solvent under vacuo the resulting amine was dissolved in 20 ml of a mixture 2 to 1 of methanol and a buffered solution of acetic acid and sodium acetate at pH=5.3. A 37% solution of formaldehyde in water (1.16 mmol) was added and the mixture was stirred at room temperature for 1 hour. Then sodium cyanoborohydride (1.16 mmol) was added and the mixture was stirred over night at room temperature. The methanol was removed under vacuo and the water was eliminated by liophylisation. The solid obtained was purified by flash chromatography to yield ethyl 3-methyl-5-(4-methyl-morpholin-2-ylmethoxy)-benzofuran-2-carboxylate: m/z=334 in MS ES+, as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915300B2
Source datasetuspto-grants-2011_03
ORD IDord-7db421f564a64c2590ae67e10d6442cb
Source noteuspto-grants-2011_03