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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235344Generated: October 25, 2026

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

https://huagongshe.com/reaction/235344

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 min 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% /PrNH2 /CH2Cl2 followed by a gradient of /PrNH2 /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 numberUS05597928
Source datasetuspto-grants-1997_01
ORD IDord-7fa9a543ff6a42ba8c85a7a23afb39d9
Source noteuspto-grants-1997_01