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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490217Generated: October 29, 2026

(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinone → HCID 21480638, compound

https://huagongshe.com/reaction/1490217

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinoneHCID 21480605—
Reactant3-Bromo-5-(((tert-butyldimethylsilyl)oxy)methyl)pyridineHCID 21984091—
ProductHCID 21480638HCID 2148063862%

Reaction Steps

Using a procedure similar to that described in example 1 except starting with 1-(9,10-dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinone (described in example 5d) and employing 3-bromo-5-(tert-butyldimethylsilyl)oxymethylpyridine (described in example 69b), the title compound was formed in 62% yield as an oil. TLC analysis (Rf 0.25, 30% ethyl acetate in hexane). MS (CI, CH4) m/z 527 (M+1,100), 555 (M+29,14), 509 (20),395 (20)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681840
Source datasetuspto-grants-1997_10
ORD IDord-50c564206002423aa7d10a802cfedd1a
Source noteuspto-grants-1997_10