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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271333Generated: November 1, 2026

Piperidine → HCID 70979664, compound

https://huagongshe.com/reaction/2271333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 86717739HCID 86717739—
SolventEthanolHCID 702—
ProductHCID 70979664HCID 7097966494.8%

Reaction Steps

Preparation according to Example 1 but performed in one portion: 1-(2-bromoethoxy)-3-fluoro-5-methylsulfonyl-benzene (0.5 g, 1.68 mmol) and piperidine (1.33 ml, 13.46 mmol) in ethanol (5 ml). Purification by flash column chromatography (ethyl acetate/methanol, 100:0 to 85:15) gave the title compound (480 mg, 94.7%). The amine was converted to the hydrochloric acid salt and re-crystallized from methanol/diethyl ether: M.p. 194.6° C. MS m/z (relative intensity, 70 eV) 301(M+, 1), 99 (8), 98 (bp), 96 (4), 55 (5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120728B2
Source datasetuspto-grants-2015_09
ORD IDord-8260de044b534d959a9cee3933eca8a6
Source noteuspto-grants-2015_09