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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781188Generated: November 1, 2026

Benzyl Bromide → [(1-Nitrocyclohexyl)methyl]benzene

https://huagongshe.com/reaction/1781188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantNitrocyclohexaneHCID 14285—
ReactantSodium hydrideHCID 24758—
Product[(1-Nitrocyclohexyl)methyl]benzeneHCID 4560895—

Reaction Steps

Nitrocyclohexane and benzylbromide are subjected to condensation reaction in the presence of sodium hydride to obtain 1-benzyl-1-nitrocyclohexane. The product is reduced with lithium aluminum hydride to obtain 1-benzyl-1-aminocyclohexane. The product is reacted with methyl chloroformate to obtain 1-benzyl-1-methoxycarbonylaminocyclohexane, and the product is subjected to intramolecular cyclization in the presence of phosphorous oxychloride to obtain spiro[1,2,3,4-tetrahydroisoquinoline-2,1'-cyclohexan]-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631363
Source datasetuspto-grants-1997_05
ORD IDord-8ffa93c5ef86417abed9b6bb2c6c17f9
Source noteuspto-grants-1997_05