HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pentafluorophenyl Trifluoroacetate → HCID 59730658, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pentafluorophenyl Trifluoroacetate | HCID 4327891 | — |
| Reactant | 3-[(tert-Butyl)oxycarbonyl]propyl phenylmethyl butane-1,4-dioate | HCID 59730696 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59730658 | HCID 59730658 | 91% |
Reaction Steps
Compound 3 (2.0 g, 5.7 mmol) was hydrogenated for 20 h at 40 psi in THF (100 mL) in the presence of 0.2 g of 10% Pd/C. The catalyst was removed by filtration through Celite and filtrate concentrated. The acid was dissolved in 20 mL of anhydrous CH2Cl2. Diisopropylethylamine ((0.88 g, 6.8 mmol) was added followed by pentafluorophenyl trifluoroacetate (1.9 g, 6.8 mmol). After being kept at room temperature for 1 h solvent was evaporated and residue chromatographed on silica (ethyl acetate-hexane) to afford 2.2 g (91%) of 4 as viscous liquid. 1H NMR (DMSO-d6) δ 4.05 (t, J=6 Hz, 2H), 3.04 (t, J=6 Hz, 2H), 2.72 (t, J=6 Hz, 2H), 2.26 (t, J=7 Hz, 2H), 1.78 (q, 2H), 1.38 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07381818B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-3895e331c8d948d79438e421802a7a6a |
| Source note | uspto-grants-2008_06 |