HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (R)-1-(4-dodecylbenzoyl)pyrrolidine-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Dodecylbenzoic acid | HCID 413311 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | tert-butyl (2R)-2-cyanopyrrolidine-1-carboxylate | HCID 2756788 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-1-(4-dodecylbenzoyl)pyrrolidine-2-carbonitrile | HCID 53248516 | 39.3% |
Reaction Steps
General procedure D was used to deprotect 1.4 mmols of 41 using 14 mL of dichloromethane and trifluoroacetic acid. After previously described recrystallization techniques, the TFA salt of 41 was coupled to 0.4 grams (1.4 mmols) of 4-dodecylbenzoic acid using 0.73 grams (1.4 mmols) of PyBOP and 0.72 grams (5.6 mmols) of N,N-diisopropylethylamine in 14 mL of dichloromethane according to general procedure E. Using previously described work-up and purification techniques (column chromatography, 25% EtOAc in hexanes), yielded 0.2 grams (0.55 mmols, 39%) of the title product as an off-white solid. 1H and 13C NMR data were identical to that of 29.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09421177B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-8578b2e9775f4dc9abbc0d363edf4e0d |
| Source note | uspto-grants-2016_08 |