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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128642Generated: October 29, 2026

Hexane → HCID 21474126, compound

https://huagongshe.com/reaction/128642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21474134HCID 21474134—
SolventFormic AcidHCID 284—
SolventFormaldehydeHCID 712—
ProductHCID 21474126HCID 2147412676%

Reaction Steps

Dissolved 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)piperidine (0.75 g, 2.7 mmol)in 1.1 mL of formic acid and 1.5 mL of 37% aqueous formaldehyde. Heated in a 90°-95° C. oil bath for 20 hours. Cooled to room temperature, and made basic with 5% NaOH. Extracted with ether. Dried combined organic extracts with MgSO4, filtered, and evaporated. Crystallized product from hexane to give 0.60 g (76% yield) of 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-l-methyl-piperidine as white solid. Dissolved the free base in ether, and added 19 weight % HCl-EtOH to precipitate the hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464840
Source datasetuspto-grants-1995_11
ORD IDord-cbaf44fe25ae4421aa889d5112569218
Source noteuspto-grants-1995_11