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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507222Generated: November 1, 2026

(Diethylamino)sulfur trifluoride → HCID 118207444, compound

https://huagongshe.com/reaction/1507222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
Reactanttert-Butyl (3S,4S)-3-hydroxy-4-(4-hydroxyphenyl)piperidine-1-carboxylateHCID 24820608—
SolventDichloromethaneHCID 6344—
ProductHCID 118207444HCID 118207444—

Reaction Steps

To a solution of (3S,4S)-tert-butyl 3-hydroxy-4-(4-hydroxyphenyl)piperidine-1-carboxylate (400 mg, 1.36 mmol, the first eluting enantiomer E-1 from step E) in DCM (5 mL) cooled to 0° C. was added dropwise DAST (0.54 mL, 4.1 mmol) over 10 min. The mixture was allowed to warm up to rt and was stirred for 2 h. The reaction was slowly quenched with 50 mL of a 10% aqueous sodium bicarbonate solution and extracted four times with 50 mL of DCM. The combined organic layers were washed with 75 mL of brine, dried, and concentrated under vacuum to yield 390 mg of (3S,4S)-tert-butyl 3-fluoro-4-(4-hydroxyphenyl)piperidine-1-carboxylate which was used without further purification. LCMS (Method Q) RT 0.92 min, m/z 240.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221796B2
Source datasetuspto-grants-2015_12
ORD IDord-29e17b7b3f3e48faacfdf92390431a1b
Source noteuspto-grants-2015_12