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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376330Generated: October 31, 2026

2-Methylaziridine → HCID 23114148, compound

https://huagongshe.com/reaction/2376330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylaziridineHCID 6377—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 23113955HCID 23113955—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23114148HCID 2311414899%

Reaction Steps

To a solution of (2-(4-isopropylbenzyl)-3,5-dimethylphenoxy)acetic acid obtained in Reference Example 157 (9.00 g, 28.8 mmol) in THF (90 mL) was added dropwise oxalylchloride (3.77 mL, 43.2 mmol) with ice-cooling, and was then added DMF (four drops), and then the mixture was stirred for 30 minutes. The reaction solution was stirred at room temperature for 30 minutes, and the solvent was distilled off under reduced pressure. To a solution of propyleneimine (1.97 g, 34.6 mmol) and triethylamine (4.82 mL, 34.6 mmol) in THF (80 mL) was added dropwise the obtained solution of acid chloride in THF (100 mL) with ice-cooling. The mixture was stirred for 30 minutes, and then was warmed to room temperature, and water was added to the reaction solution, which was extracted with ethyl acetate. The combined organic layer was washed with a saturated brine, dried over sodium sulfate, and then concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=2:3) to obtain 10.0 g (yield 99%) of the title compound. Oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465815B2
Source datasetuspto-grants-2008_12
ORD IDord-e8479396218947ec81cbd2a9209f444c
Source noteuspto-grants-2008_12