Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460639Generated: October 29, 2026

2,6-Dimethylaniline → HCID 15680270, compound

https://huagongshe.com/reaction/1460639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DimethylanilineHCID 6896—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 15680272HCID 15680272—
SolventBenzeneHCID 241—
ProductHCID 15680270HCID 15680270—

Reaction Steps

The title compound of Example 11 (2.3 g, 0.0068 mole) was dissolved in benzene and the solution cooled to +10° C. in an ice bath. A solution of oxalyl chloride (1.14 g, 0.009 mole) in benzene (10 ml) was added dropwise over a period of 20 minutes. The ice bath was removed and the solution stirred at room temperature for 12 hours. The benzene was removed, fresh benzene (10 ml) added and the procedure repeated. The residue was taken up in benzene and a solution of 2,6-dimethylaniline (0.84 g, 0.007 mole) in benzene (25 ml) added over a period of 20 minutes, followed by the dropwise addition of a solution of triethylamine (1 ml). The solution was stirred for 4 hours and the benzene removed. The residue was taken up in ethyl ether (100 ml), stirred, and the white solid filtered. The filtrate was stripped and the product purified by chromatography on silica. The product was recrystallized from ethyl acetate/hexane, filtered and dried, m.p. ca. 137°-139.5° C. Analysis calc. for C27H39NO2S(441.67): Calc.: C, 73.43; H, 8.90; N, 3.17; S, 7.26. Found: C, 73.75; H, 8.90; N, 3.12; S, 7.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05071876
Source datasetuspto-grants-1991_12
ORD IDord-dcb9770c757f4499b4b3c71da64c7313
Source noteuspto-grants-1991_12