HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,3,5,6-Tetrafluorophenyl 6-{[(4-methoxyphenyl)diphenylmethyl]amino}hexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,3,5,6-Tetrafluorophenyl trifluoroacetate | HCID 15334258 | — |
| Reactant | ([(4-Methoxyphenyl)diphenylmethyl]amino}hexanoic acid, triethylammonium salt | HCID 131726683 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3,5,6-Tetrafluorophenyl 6-{[(4-methoxyphenyl)diphenylmethyl]amino}hexanoate | HCID 18408168 | — |
Reaction Steps
The acid 6 obtained as described above (2.2 g, 4.4 mmol) was dissolved in anhydrous CH2Cl2 and treated with 1 ml of triethylamine followed by 0.8 ml of 2,3,5,6-tetrafluorophenyltrifluoroacetate. After being kept at room temperature for 30 min, the reaction was concentrated to an oil (crude 7), which then was re-suspended in 20% ethyl acetate/80% hexane and applied to a silica gel column. Elution with 15% ethyl acetate/85% hexane and concentration of the pure product fractions afforded 2.0 g (82%) of the TFP ester (7) as a colorless, viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07297495B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-474c7fb7d18a4b00a575706a805ec96b |
| Source note | uspto-grants-2007_11 |