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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204122Generated: November 2, 2026

Hydrochloric Acid → 1-methyl-1H-spiro[chromeno[4,3-b]pyrrole-4,4'-piperidine]

https://huagongshe.com/reaction/2204122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1-DichloroethaneHCID 6365—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Reactant2-(1-Methyl-1H-pyrrol-2-yl)phenolHCID 22090448—
Product1-methyl-1H-spiro[chromeno[4,3-b]pyrrole-4,4'-piperidine]HCID 58551840—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-(1-methylpyrrol-2-yl)phenol (1.20 g, 6.90 mmol), tert-butyl 4-oxopiperidine-1-carboxylate (1.38 g, 6.93 mmol), 4-methylbenzenesulfonic acid hydrate (264 mg, 1.39 mmol), and dichloroethane (24 mL) was heated at 80° C. for 2 h. To the mixture was added HCl (1.7 mL of 4.0 M, 6.9 mmol) and the mixture was allowed to stir at 50° C. for 1 h. The mixture was cooled to 25° C. and was concentrated in vacuo. The residue was taken up in dichloromethane and was washed with saturated aqueous NaHCO3. The organic layer was dried over sodium sulfate and concentrated. Column chromatography (0-100% ethyl acetate/hexanes) on the residue gave 1-methyl-1H-spiro[chromeno[4,3-b]pyrrole-4,4′-piperidine]. ESI-MS m/z calc. 254.3, found 255.2 (M+1)+; Retention time: 1.51 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-dc305335409844eb8b4b06b6fb052359
Source noteuspto-grants-2016_06