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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011351Generated: November 2, 2026

Ammonium Chloride → HCID 58478817, compound

https://huagongshe.com/reaction/1011351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 58478784HCID 58478784—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58478817HCID 58478817—
ProductHCID 58478846HCID 58478846—

Reaction Steps

To a suspension of (methoxymethyl) triphenylphosphonium chloride (889 mg, 2.6 mmol) in anhydrous THF (10 mL) is added slowly to a solution of potassium tert butoxide in tBuOH (2.4 mL of a 1.0 M solution in tBuOH, 2.4 mmol) under an argon atmosphere. The brown reaction mixture is stirred at room temperature for 30 min, cooled to 0° C. and treated with 5-oxo-5,7-dihydro-furo[3,4-b]pyridine-2-carbaldehyde (326 mg, 2.0 mmol) in one portion. The dark brown reaction mixture is stirred at room temperature for 3 h and then poured into saturated aqueous NH4Cl solution (30 mL). The reaction mixture is extracted with EtOAc (2×). The combined organic extracts are dried Na2SO4, filtered and concentrated. The residue is purified by chromatography (silica gel, EtOAc/hexane) to give the higher Rf E-isomer, E-2-(2-Methoxy-vinyl)-7H-furo[3,4-b]pyridin-5-one (111 mg, 0.58 mmol) and lower Rf Z-isomer, Z-2-(2-Methoxy-vinyl)-7H-furo[3,4-b]pyridin-5-one (61 mg, 0.32 mmol). Total yield is 45%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977351B2
Source datasetuspto-grants-2011_07
ORD IDord-da19f07b7d9446908f3a7418087a73ca
Source noteuspto-grants-2011_07