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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254685Generated: November 1, 2026

Triphenylphosphine → HCID 67005931, compound

https://huagongshe.com/reaction/1254685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 67006584HCID 67006584—
SolventDichloromethaneHCID 6344—
ProductHCID 67005931HCID 6700593184%

Reaction Steps

Triphenylphosphine (590 mg, 2.25 mmol) was dissolved in 25 mL of DCM followed by addition of 12 (571 mg, 2.25 mmol) and TEA (456 mg, 4.50 mmol) at 0° C. N′-((2R,3R)-3-(tert-butyldimethylsilyloxy)-2-(4-cyano-2-methyl-3-(trifluoromethyl)phenylamino)butanoyl)-4-cyanobenzohydrazide (630 mg, 1.13 mmol) in 25 mL DCM was added to the pre-cooled solution mixture of PPh3/I2/TEA system and stirred. The temperature was allowed to rise to room temperature and stirred for additional 10 min. The reaction was quenched with 50 mL saturated sodium thiosulfate and extract with EtOAc. The crude mixture was chromatographed to give the product (510 mg, 84%) 1H NMR (400 MHz, acetone-d6, δ in ppm): 8.23 (d, J=9 Hz, 2H), 8.04 (d, J=9 Hz, 2H), 7.67 (d, J=9 Hz, 1H), 7.27 (d, J=9 Hz, 1H), 5.94 (d, J=9 Hz, 1H), 5.19 (m, 1H), 4.74 (m, 1H), 2.39 (m, 3H), 1.48 (d, J=6 Hz, 3H), 0.81 (s, 9H), 0.12 (s, 3H), 0.00 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455525B2
Source datasetuspto-grants-2013_06
ORD IDord-dc50e1f9226344c0822667c6db2b2b1f
Source noteuspto-grants-2013_06