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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618948Generated: November 1, 2026

Chloroform → HCID 86707002, compound

https://huagongshe.com/reaction/1618948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 6-bromo-3-hydroxypicolinateHCID 22175135—
SolventWaterHCID 962—
ProductHCID 86707002HCID 86707002100%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diisopropylethylamine (1.46 mL) was added to a chloroform (20 mL) solution of methyl 6-bromo-3-hydroxypyridine-2-carboxylate (970 mg) and placed in a nitrogen atmosphere. Next, the reaction mixture was cooled to 0° C., and chloromethoxymethane (0.38 mL) was added thereto. The reaction mixture was stirred at 0° C. for 5 minutes, and then stirred at room temperature for 1 hour. The reaction mixture was cooled to 0° C., diluted with water, and extracted with chloroform. The combined organic layer was washed with saturated sodium chloride, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (hexane:ethyl acetate) to give the desired product (1.22 g, yield: 100%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772283B2
Source datasetuspto-grants-2014_07
ORD IDord-35c4a9e11a0d4bc6a8102d365ada98ff
Source noteuspto-grants-2014_07