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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460373Generated: October 30, 2026

Dimethylformamide → HCID 22933011, compound

https://huagongshe.com/reaction/460373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22485495HCID 22485495—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 22933011HCID 2293301197.3%

Reaction Steps

To a solution of 4-iodo-2,6-dimethoxybenzoic acid (603.0 mg, 1.96 mmol), synthesized by the process described in Reference Example 11, in methylene chloride (12 mL) were added dimethylformamide (0.020 mL, 0.26 mmol) and oxalyl chloride (0.26 mL, 3.0 mmol). After stirring at room temperature for 30 minutes, the resulting solution was poured into an ice-cold solution of triethylamine (0.50 mL, 3.6 mmol) in ethanol (10 mL). The reaction mixture was stirred at room temperature for 30 minutes and concentrated under reduced pressure. A solution of the residue in diethyl ether was washed successively with water, 0.1 M hydrochloric acid and brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to yield the title compound as a colorless oil (641.0 mg, yield: 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196101B2
Source datasetuspto-grants-2007_03
ORD IDord-39fe97f5706d4f15be43ba7276fd11f7
Source noteuspto-grants-2007_03