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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632005Generated: October 29, 2026

Triethylamine → 2-(3-Methyl-1,2-oxazol-5-yl)propan-2-amine

https://huagongshe.com/reaction/632005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Butyn-2-amine, 2-methyl-HCID 76319—
Reactant(E)-Acetaldehyde oximeHCID 5324279—
ReactantSodium HypochloriteHCID 23665760—
SolventDichloromethaneHCID 6344—
Product2-(3-Methyl-1,2-oxazol-5-yl)propan-2-amineHCID 674635744.2%

Reaction Conditions

Temperature4 °C

Reaction Steps

To a solution of (E)-acetaldehyde oxime (CAN 107-29-9, 1.0 g, 16.9 mmol), 2-methylbut-3-yn-2-amine (CAN 2978-58-7, 1.4 g, 16.9 mmol) and triethylamine (CAN 121-44-8, 0.17 g, 1.69 mmol) in methylene chloride (25 mL) at 0° C. was added a 5% aqueous solution of sodium hypochlorite (5%, 42.6 g) over 3 h. The reaction was allowed to warm to 4° C. and stirring continued for 5 h. The organic layer was separated, and the aqueous layer was extracted with methylene chloride (50 mL). The combined methylene chloride extracts were washed with saturated aqueous sodium chloride (60 mL) and dried over anhydrous magnesium sulfate. The solvent was removed to give a yellow oil. The crude product was purified by column chromatography (silica gel 30 g, eluting with 30% ethyl acetate in petroleum ether) to yield the product as yellow solid (0.1 g, 4.2%); MS (EI): m/e=141.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321727B2
Source datasetuspto-grants-2016_04
ORD IDord-bf0412a7d10a417090353e11af540397
Source noteuspto-grants-2016_04