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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484091Generated: October 30, 2026

Trifluoroacetic acid → (R)-1-(4-dodecylbenzoyl)pyrrolidine-2-carbonitrile

https://huagongshe.com/reaction/1484091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Dodecylbenzoic acidHCID 413311—
ReactantPyBOPHCID 2724699—
Reactanttert-butyl (2R)-2-cyanopyrrolidine-1-carboxylateHCID 2756788—
SolventDichloromethaneHCID 6344—
Product(R)-1-(4-dodecylbenzoyl)pyrrolidine-2-carbonitrileHCID 5324851639.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09421177B2
Source datasetuspto-grants-2016_08
ORD IDord-8578b2e9775f4dc9abbc0d363edf4e0d
Source noteuspto-grants-2016_08