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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366485Generated: October 26, 2026

Trifluoroacetic acid → 4-[5-Fluoro-1-(2-trimethylsilylethanesulfonyl)indol-3-yl]piperidine

https://huagongshe.com/reaction/366485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-tert-butoxycarbonyl-4-[5-fluoro-1-(2-trimethylsilylethanesulfonyl)indol-3-yl]piperidineHCID 22615698—
SolventDichloromethaneHCID 6344—
Product4-[5-Fluoro-1-(2-trimethylsilylethanesulfonyl)indol-3-yl]piperidineHCID 22615720100%

Reaction Steps

To a solution of N-tert-butoxycarbonyl-4-(5-fluoro-1-(2-trimethylsilylethane-sulfonyl)indol-3-yl]piperidine (1.33 g, 2.73 mmol), [prepared as described in Step 2, above] in methylene chloride (3 ml), was added trifluoroacetic acid (4 ml). After 2 h, the reaction mixture was concentrated in vacuo and the residue was partitioned between methylene chloride (50 ml) and of 1M NaOH (10 ml). The organic layers were dried over MgSO4 and concentrated in vacuo to afford 4-[5-fluoro-1-(2-trimethylsilylethanesulfonyl)indol-3-yl]piperidine (100%). This material was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130220
Source datasetuspto-grants-2000_10
ORD IDord-1461e1dbb09348a7a52b5247136f68f1
Source noteuspto-grants-2000_10