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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367543Generated: October 25, 2026

Sodium Iodide → (1R,2R,4S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-[4-(4-fluoro-phenyl)-piperidin-1-ylmethyl]-cyclopentanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/1367543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactant4-(4-Fluorophenyl)piperidineHCID 2759136—
Reactant(1R,2R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonyloxymethyl)-cyclopentanecarboxylic acid ethyl esterHCID 86649030—
SolventDimethylformamideHCID 6228—
Product(1R,2R,4S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-[4-(4-fluoro-phenyl)-piperidin-1-ylmethyl]-cyclopentanecarboxylic acid ethyl esterHCID 6691895141%

Reaction Steps

A solution of (1R,2R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonyloxymethyl)-cyclopentanecarboxylic acid ethyl ester (example 148, step 1, epimeric mixture, 410 mg), 4-(4-Fluoro-phenyl)-piperidine (cas # 6716-98-9, 291 mg), sodium iodide (1.36 g) and triethylamine (545 mg) in N,N-dimethylformamide (2.8 mL) was stirred at 90° C. over 6 h. The reaction mixture was partitioned between ethyl acetate and an aqueous saturated solution of sodium hydrogenocarbonate. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel with a gradient of cyclohexane/ethyl acetate (9:1 to 1:1 v/v) as eluant to afford the title compound (170 mg, 41%) as a yellow liquid. MS (EI): 464.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893099B2
Source datasetuspto-grants-2011_02
ORD IDord-ef2dabc918964390ba7163f2db9c7f55
Source noteuspto-grants-2011_02