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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891676Generated: November 1, 2026

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

https://huagongshe.com/reaction/1891676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantLithium methanolateHCID 4177230—
Reactant2-Chloro-5-(4-(2-nitro-ethyl)-benzyl)furanHCID 59255322—
CatalystTitanium TetrachlorideHCID 24193—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(4-(5-Chloro-furan-2-ylmethyl)-phenyl)-acetohydroximoyl chlorideHCID 7226285184%

Reaction Steps

To a mixture of 2-chloro-5-(4-(2-nitro-ethyl)-benzyl)furan (100 mg, 0.38 mmol) described in Manufacturing Example 62-1-5 and methanol (2 mL) was added lithium methoxide (29 mg, 0.75 mmol) at room temperature, which was stirred for 10 minutes at room temperature. The solvent was evaporated from the reaction mixture under a reduced pressure. Titanium (IV) chloride (91 μL, 0.83 mmol) was added at −78° C. to a mixture of the resulting residue, methylene chloride (2 mL) and tetrahydrofuran (1 mL), and stirred for 1 hour at 0° C. The reaction mixture was cooled to −78° C., water (1 mL) was added, and the temperature was gradually raised to room temperature. Ethyl acetate and water were added to extract the reaction mixture. The organic layer was washed with water until the pH became roughly 5. The organic layer was washed with saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate. The organic layer was concentrated under a reduced pressure to obtain the title compound (110 mg, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-19ede51598764375abe10715fe7300e0
Source noteuspto-grants-2013_08