HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 4-(2-(11-carbomethoxyundecanoylamino)phenoxy)butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-(2-aminophenoxy)butanoate | HCID 11816929 | — |
| Reactant | Dodecanedioic acid, monomethyl ester | HCID 22672980 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 4-(2-(11-carbomethoxyundecanoylamino)phenoxy)butyrate | HCID 18796179 | 85% |
Reaction Steps
To a stirred, ice-cold solution of 0.89 g (4.0 mM) amine (4) and dried triethylamine (1.2 mL) in dry ether (40 mL) is added dropwise over ca. 4 minutes a solution of acid chloride (7) (1.04 g, 4.6 mM) in 20 mL of dry ether. The resultant mixture is allowed to stir cold for 20 minutes, and then at room temperature overnight. After filtering off the triethylamine hydrochloride, the ether filtrate is concentrated in vacuo and the residue chromatographed on an 82 g silica gel column using 20% ethyl acetate/hexane as eluant to give 1.49 g (85%) of (8) as a waxy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753641 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-ae30085c40a5482da54bc84ad2151343 |
| Source note | uspto-grants-1998_05 |