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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440619Generated: November 3, 2026

Carbon Dioxide → HCID 21475509, compound

https://huagongshe.com/reaction/440619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
Reactant6-(Dimethylamino)hexanoic acid hydrochlorideHCID 19977751—
ProductHCID 21475509HCID 21475509—

Reaction Conditions

Temperature30 °C

Reaction Steps

Oxalyl chloride (3367.33 g, 26.53 mol) is placed in a 5000 mL three-necked round-bottomed flask equipped with a reflux condenser, internal thermometer, mechanical stirrer, and argon inlet. 6-(N,N-Dimethylamino)hexanoic acidhydrochloride (1146.00 g, 5.86 mol) is added over 3 h while maintaining the reaction temperature between 25-35 ° C. As reaction takes place, HCl, CO2, and CO are swept away from the mixture with argon. After addition is complete, the mixture is cooled to room temperature over 45 min. Excess oxalyl chloride is removed first by rotary evaporation at 50° C. (water aspirator vacuum) and then by Kugelrohr distillation at 60° C. (0.3 mm Hg) for 3 h. A quantitative yield of 3 is isolated as a dark red oil that solidifies on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05520835
Source datasetuspto-grants-1996_05
ORD IDord-1e1d38c615d940ce82dc5f522df2c864
Source noteuspto-grants-1996_05