Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508286Generated: October 31, 2026

4-Nitrophenol → HCID 131734381, compound

https://huagongshe.com/reaction/1508286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantL-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDichloromethaneHCID 6344—
ProductHCID 131734381HCID 131734381—

Reaction Steps

To a mixture of Boc-L-phenylalanine (1.33 g, 5 mmol), p-nitrophenol (PNP) (838 mg, 6 mmol) and DIPEA (1.75 ml, 10 mmol) in anhydrous DCM (10 mL) was added HATU (2.28 g, 6 mmol) in one portion under a nitrogen atmosphere. The resulting mixture was stirred at room temperature for 4 h. After aqueous work-up the crude product was purified by flash column chromatography (silica gel, 0-20% EtOAc/hexanes) to give Boc-L-phenylalanine-PNP ester (R-40). To an ice-cooled mixture of R-101 (54 mg, 0.1 mmol) and R-40 (77 mg, 0.2 mmol) in anhydrous THF (2 mL) was added LiHMDS (0.15 mL of 1M solution in THF, 0.15 mmol) dropwise under a nitrogen atmosphere. The resulting mixture was stirred at the same temperature for 2 h. The reaction mixture was quenched with saturated ammonium chloride solution and extracted with DCM. The combined organic extracts were dried over MgSO4, filtered and concentrated. The crude material was purified by flash column chromatography (silica gel, 0-5% MeOH/DCM) to give R-41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221831B2
Source datasetuspto-grants-2015_12
ORD IDord-dd417b1de2f246e8b46b465715f02fc4
Source noteuspto-grants-2015_12