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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2-(Methyl(4-(methylsulfonamido)benzyl)amino)acetic acid hydrochloride | HCID 86679453 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Allyl 2-(methyl(4-(methylsulfonamido)benzyl)amino)acetate | HCID 86679455 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09265768B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-f503b6d95e6b42899920f547adecedf7 |
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| Source note | uspto-grants-2016_02 |
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