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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903352Generated: November 1, 2026

Triethylamine → HCID 20468635, compound

https://huagongshe.com/reaction/1903352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chlorideHCID 3017765—
ReactantN-MethylaminoethanolHCID 5247031—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20468635HCID 2046863538.9%

Reaction Steps

5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoyl chloride (7 g, 0.0184 mole) was added over 1 hr to a solution of N-methylaminoethanol (2.8 g, 0.0372 mole), triethylamine (3.7 g, 0.0368 mole) and THF (30 ml) at 25°-38°. The resulting mixture was heated to and held at reflux for 1.5 hrs., cooled and concentrated. The residue was taken into 400 ml of ether, washed three times with water, dried over MgSO4 and concentrated to 7.8 g of crude product. Kugelrohr distillation under reduced pressure afforded 3.0 g of pure N-(2-Hydroxyethyl)-N-methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide as a gum; nmr (CDCl3) δ 2.95-3.08 (2S, 3H); 3.22-3.82 (m) 4.74 (s, 1H), 7.04-8.52 (m, 6H); ir (CHCl3) 3640, 3420, 1648 Cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435588
Source datasetuspto-grants-1984_03
ORD IDord-286be7e07d8f48a9bba9c35cad4dcd67
Source noteuspto-grants-1984_03