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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776506Generated: November 1, 2026

Allyl Alcohol → Allyl 2-(methyl(4-(methylsulfonamido)benzyl)amino)acetate

https://huagongshe.com/reaction/1776506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-(Methyl(4-(methylsulfonamido)benzyl)amino)acetic acid hydrochlorideHCID 86679453—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductAllyl 2-(methyl(4-(methylsulfonamido)benzyl)amino)acetateHCID 8667945588%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 2-(methyl(4-(methylsulfonamido)benzyl)amino)acetic acid hydrochloride (1.054 g, 3.41 mmol), CDI (1.107 g, 6.83 mmol), and TEA (0.952 ml, 6.83 mmol) in CH3CN (80 ml) was heated at 75° C. for 3 hours. The solvent was evaporated; the residue was dissolved in prop-2-en-1-ol (30 ml, 439 mmol) and heated at 75° C. for 1 hour. The mixture was diluted with EtOAc and washed several times with NH4Cl sat. sol. The organic phase was dried over Na2SO4, the solvent was removed, and the residue was filtered on SCX cartridge (DCM/MeOH 1/1; conc.aq.NH4OH/MeOH 1/9). The basic fraction was evaporated to dryness to give allyl 2-(methyl(4-(methylsulfonamido)benzyl)-amino)acetate as a brown oil (0.942 g, 3.02 mmol, 88% yield, MS/ESI+ 313.2 [MH]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265768B2
Source datasetuspto-grants-2016_02
ORD IDord-f503b6d95e6b42899920f547adecedf7
Source noteuspto-grants-2016_02