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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118236Generated: October 30, 2026

Oxalyl chloride → HCID 178483791, compound

https://huagongshe.com/reaction/2118236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
ReactantHCID 178484815HCID 178484815—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 178483791HCID 17848379153%

Reaction Steps

A solution of 0.137 g (0.375 mmol) of trans-4-[methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexanecarboxylic acid in 2 mL of CH2Cl2 was treated at RT with 1 drop of DMF, followed by 0.035 mL (0.412 mmol, 1.1 eq) of oxalyl chloride within 5 min, and stirring was continued for 90 min. The solution was evaporated, redissolved in 2 mL of CH2Cl2 and treated with 0.058 mL (0.450 mmol, 1.2 eq) of N,N,N′-trimethylethylenediamine at 0° C. The reaction was kept at RT for 2 h, then partitioned between Et2O (×3)/aqueous saturated NaHCO3. The organic phases were washed once with 10% aqueous NaCl, dried over Na2SO4 and evaporated. Purification by flash-chromatography on 8 g of silica gel (CH2Cl2:MeOH 99:1 to 9:1) gave 0.088 g (53%) of pure trans-4-[methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexanecarboxylic acid (2-dimethylamino-ethyl)-methyl-amide, MS: 450 (MH+), MP: 83° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442791B2
Source datasetuspto-grants-2008_10
ORD IDord-c9605360ea4543a29c28e69b32155622
Source noteuspto-grants-2008_10