HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601333Generated: October 26, 2026
2-(Dimethylamino)ethanol → 2-Dimethylaminoethyl docosahexaenoate
https://huagongshe.com/reaction/1601333
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Dimethylamino)ethanol | HCID 7902 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Docosahexenoic acid | HCID 175542 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Dimethylaminoethyl docosahexaenoate | HCID 54390294 | 92% |
Reaction Steps
To a solution of docosahexaenoic acid (0.986 g, 3.0 mmol) in CH3CN (6.0 mL) was added carbonyldiimidazole (0.535 g, 3.3 mmol) in one portion at 0° C. The mixture was allowed to warm to room temperature and stirred at room temperature for 30 min. TLC showed a complete reaction (1:1 EtOAc/hexane). N,N-dimethylaminoethanol (0.89 g, 10.0 mmol) was added dropwise followed by addition of 4-dimethylaminopyridine (0.073 g, 0.60 mmol) The mixture was stirred at room temperature overnight. The solvent was removed by rotary evaporation and the residue was purified on silica gel using 72% EtOAc/hexane, 80% EtOAC/hexane and 100% EtOAc with 0.5% MeOH each to provide the product, 2-dimethylaminoethyl docosahexaenoate (1.098 g, 92%), as a light yellow oil. The product was stored at -20° C. with small amount of β-carotene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977174 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-723829f3630e452dba5f39a9f2acb84c |
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| Source note | uspto-grants-1999_11 |
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