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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174883Generated: October 30, 2026

Sodium Iodide → HCID 58160391, compound

https://huagongshe.com/reaction/2174883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHCID 58160410HCID 58160410—
SolventAcetonitrileHCID 6342—
ProductHCID 58160391HCID 58160391—

Reaction Steps

122 mg (3R/S,5S)-5-Biphenyl-4-ylmethyl-2-oxo-3-(toluene-4-sulfonyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (11-a, R1=Boc, R4=Tosyl) prepared according to Example 49, Method 2 is added to acetonitrile (3 ml). Sodium iodide (105 mg) is then added to the mixture. The resulting mixture is heated at reflux overnight. The mixture is then concentrated under reduced pressure. Purification by column chromatography, eluting with ethyl acetate-heptane (1:1) gives (3R/S,5S)-5-biphenyl-4-ylmethyl-3-iodomethyl-pyrrolidin-2-one (12-a, R1=H, R5=I). 1H NMR (CDCl3): 2.13 (2H), 2.69 (2H), 2.82 (1H), 3.28 (1H), 3.35 (1H), 3.85 (1H), 5.84 (1H), 7.17 (2H), 7.28 (1H), 7.37 (2H), 7.49 (4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061973B2
Source datasetuspto-grants-2015_06
ORD IDord-a6cbe0698ccb4d6e99257b6e8fc5a5ec
Source noteuspto-grants-2015_06