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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(4-Fluorophenyl)piperidine | HCID 2759136 | — |
| Reactant | (1R,2R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-(toluene-4-sulfonyloxymethyl)-cyclopentanecarboxylic acid ethyl ester | HCID 86649030 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1R,2R,4S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-[4-(4-fluoro-phenyl)-piperidin-1-ylmethyl]-cyclopentanecarboxylic acid ethyl ester | HCID 66918951 | 41% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893099B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-ef2dabc918964390ba7163f2db9c7f55 |
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| Source note | uspto-grants-2011_02 |
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