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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905559Generated: November 2, 2026

Water → 2,2-Dichloro-N-[(2-ethoxyethoxy)methyl]-N-(3-methylbutyl)acetamide

https://huagongshe.com/reaction/1905559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantGlycol monoethyl etherHCID 8076—
ReactantTriethylamineHCID 8471—
Reactant2,2-Dichloro-N-(chloromethyl)-N-(3-methylbutyl)acetamideHCID 20035849—
SolventBenzeneHCID 241—
Product2,2-Dichloro-N-[(2-ethoxyethoxy)methyl]-N-(3-methylbutyl)acetamideHCID 13824294—

Reaction Steps

The solution of N-isopentyl-N-chloromethyldichloroacetamide (24.7 g., 0.1 mole) and 2-ethoxyethanol (9.9 g., 10.7 ml., 0.11 mole) in dry benzene (70 ml) is weighed in a four-necked, round-bottom flask of 250 ml, equipped with a calcium chloride tube, reflux condenser, mechanical stirrer, dropping funnel and thermometer. Triethylamine (10.1 g., 13.9 ml., 0.1 mole) is added to this solution under stirring and cooling by water in such a rate that the temperature is maintained below 40° C. After the addition is complete, the mixture is stirred for an additional 2 hours at room temperature. The mixture is washed with water (2×100 ml.) to remove triethylamine hydrochloride and the possible hydrophilic side-product, the benzene solution is dried over anhydrous sodium sulfate after distillation of the solvent and the residue is evaporated to dry under reduced pressure to give 27.9 g. (93%) of the named product as a pale yellow oil which is of 96% purity according to analysis by gas chromatography and is directly useful for practical purposes without any purification; nD25 =1.4649.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04843177
Source datasetuspto-grants-1989_06
ORD IDord-ffab82cca99e478cae89e2ba99898984
Source noteuspto-grants-1989_06