Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891213Generated: October 29, 2026

4-Methylmorpholine → 3-allyloxycarbonylamino-N-methoxy-N-methyl-succinamic acid tert-butyl ester

https://huagongshe.com/reaction/891213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Allyloxycarbonylamino-succinic acid 4-tert-butyl esterHCID 23598659—
SolventDichloromethaneHCID 6344—
Product3-allyloxycarbonylamino-N-methoxy-N-methyl-succinamic acid tert-butyl esterHCID 2359871181%

Reaction Steps

2-Allyloxycarbonylamino-succinic acid 4-tert-butyl ester, 100, (43.4 g, 0.159 mol) is dissolved in CH2Cl2(900 mL). To this solution O,N-dimethyl-hydroxylamine hydrochloride (18.6 g, 0.191 mol), 4-Methyl-morpholine (21.0 mL, 19.3 g, 0.191 mol), and 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (36.6 g, 0.191 mol) are added. After the consumption of the starting material, the solution is washed with 1.0 N HCl (2×400 mL) and brine (1×250 mL). The organic layer is concentrated in vacuo and the residue purified over silica (hexanes/ethyl acetate 65:35) to afford 40.8 g (81% yield) of the desired product as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001899B2
Source datasetuspto-grants-2006_02
ORD IDord-776448b980944401919c3e344cfc54eb
Source noteuspto-grants-2006_02