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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640195Generated: October 29, 2026

Methanol → (4-(5-Methyl-furan-2-ylmethyl)-phenyl)acetohydroximoyl chloride

https://huagongshe.com/reaction/640195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantLithium methanolateHCID 4177230—
Reactant2-Methyl-5-(4-(2-nitro-ethyl)-benzyl)-furanHCID 59255527—
CatalystTitanium TetrachlorideHCID 24193—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(4-(5-Methyl-furan-2-ylmethyl)-phenyl)acetohydroximoyl chlorideHCID 7226286684%

Reaction Steps

To a mixture of 2-methyl-5-(4-(2-nitro-ethyl)-benzyl)-furan (87 mg, 0.36 mmol) described in Manufacturing Example 46-1-5 and methanol (2 mL) was added lithium methoxide (27 mg, 0.71 mmol) at room temperature, which was stirred for 15 minutes at room temperature. The solvent was evaporated from the reaction mixture under a reduced pressure. Titanium (IV) chloride (86 μL, 0.78 mmol) was added at −78° C. to a mixture of the resulting residue, methylene chloride (2 mL) and tetrahydrofuran (1 mL), which was stirred for 1 hour at 0° C. The reaction mixture was cooled to −78° C., water (5 mL) was added, and the temperature was gradually raised to room temperature. The reaction mixture was extracted by addition of ethyl acetate and water. The organic layer was washed with water until the pH became about 5. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. Thereafter, the organic layer was filtered and the filtrate was concentrated under a reduced pressure to obtain the title compound (79 mg, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-3f64f5c3416e49f9b5a118cc4f6eef7a
Source noteuspto-grants-2010_04