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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994431Generated: October 30, 2026

Allylamine → Methyl 3-allylamino-2-benzyloxycarbonylamino-2-methylpropionate

https://huagongshe.com/reaction/1994431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantMethyl 2-benzyloxycarbonylamino-2-methyl-3-oxopropionateHCID 85990941—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-allylamino-2-benzyloxycarbonylamino-2-methylpropionateHCID 68691822102.4%

Reaction Steps

1.237 ml (16.5 mmol) of allylamine and 0.9 g (7.48 mmol) of MgSO4 are added to a solution of 0.874 g (3.3 mmol) of methyl 2-benzyloxycarbonylamino-2-methyl-3-oxopropionate in 15 ml of DCM. The mixture is stirred at room temperature overnight. The reaction mixture was then filtered and concentrated in vacuo. 50 ml of anhydrous MeOH, 6 ml of NaCNBH3 (1.0M in THF) and 1.8 ml of acetic acid are added to the crude product. This mixture is stirred at RT for 2 h. The reaction solution is concentrated in vacuo, and then EtOAc and water are added. The organic phase is separated off and dried over MgSO4, and the solvent is removed in vacuo. Purification takes place by chromatography (25 g of SiO2, eluent MeOH/DCM (gradient 0-10%). 1.035 g of the desired product are obtained as an oil. MW=306 (calculated, monoisotopic), measured value: (M+H)+307.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652007B2
Source datasetuspto-grants-2010_01
ORD IDord-88d126e1bfe84a958c22535094d5af53
Source noteuspto-grants-2010_01