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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080522Generated: October 31, 2026

Methylamine → 1-(2-isopropyloxazol-4-yl)-N-methylmethanamine

https://huagongshe.com/reaction/1080522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-(Chloromethyl)-2-(propan-2-yl)-1,3-oxazoleHCID 2763291—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product1-(2-isopropyloxazol-4-yl)-N-methylmethanamineHCID 1082078471%

Reaction Steps

To 40% aqueous methylamine (100 mL) was added dropwise a suspension of 4-chloromethyl-2-isopropyloxazole (4.20 g, 0.0263 mol)in p-dioxane/H2O (1:1 (v/v), 20 mL) over a 25 rain period. After stirring for 45 min at ambient temperature, the volume was reduced to ca. 50 mL by rotary evaporation in vacuo, and NaCl was added. The aqueous was extracted with CHCl3 (4×100 mL), and the combined extract was dried over Na2SO4 and concentrated in vacuo. The resulting brown liquid was chromatographed on a 200 g SiO2 flash column with 2% iPrNH2 /CH2Cl2 followed by a gradient of iPrNH2 /MeOH/CH2Cl2 (0.5:2:97.5, 0.5:4:95.5). Concentration in vacuo of the product-containing fractions afforded the desired compound as a golden oil (2.89 g, 0.0187 mol, 71%): 1H NMR (CDCl3) δ1.33 (d, J=6.9 Hz, 6H), 2.46 (s, 3H), 2.99-3.14 (m, 1H), 3.64 (s, 2H), 7.42 (s, 1H). Mass spectrum: (M+H)+ =155, (M+NH4)+ =172.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580984
Source datasetuspto-grants-1996_12
ORD IDord-1b057ef0259e462a98b97c39418e1b43
Source noteuspto-grants-1996_12