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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382860Generated: November 1, 2026

Piperidine → HCID 14054320, compound

https://huagongshe.com/reaction/1382860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
ReactantHCID 14054310HCID 14054310—
ReactantCyclohexane ethylacetateHCID 21867204—
SolventTolueneHCID 1140—
SolventThionyl ChlorideHCID 24386—
ProductHCID 14054320HCID 14054320—

Reaction Steps

The reaction is carried out as in Example 1, but starting with 7-phenylbenzo[b]thiophene-5-carboxylic acid (2.5 g) in toluene (25 cc) and thionyl chloride (2.2 cc) and then triethylamine (4.15 cc) and piperidine (0.97 cc) in toluene (25 cc). After two successive chromatographies of the residue on silica gel, the first with a cyclohexane:ethyl acetate (80:10:10 by volume) mixture as the eluent and the second with a cyclohexane:ethyl acetate (70:30 by volume) mixture as the eluent, a residue is isolated, which is stirred for 1 hour in 40°-60° petroleum spirit. After filtering and drying, 1-[(7-phenylbenzo[b]thien-5-yl)carbonyl]piperidine (1.55 g), m.p. 112° C., is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808599
Source datasetuspto-grants-1989_02
ORD IDord-0de56bbb7a01437daf97e348252b755d
Source noteuspto-grants-1989_02