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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490216Generated: October 29, 2026

1-(2-Chloro-9,10-dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinone → HCID 21480582, compound

https://huagongshe.com/reaction/1490216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Chloro-9,10-dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinoneHCID 21480622—
Reactant3-Bromo-5-(((tert-butyldimethylsilyl)oxy)methyl)pyridineHCID 21984091—
ProductHCID 21480582HCID 2148058251%

Reaction Steps

Using a procedure similar to that described in example 1 except employing 3-bromo-5-(tert-butyldimethylsilyl)oxymethylpyridine (described in example 69b) and 1-(2-chloro-9,10-dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinone (described in example 1m), the title compound was formed in 51% yield as an oil. TLC analysis (Rf 0.20, 25% ethyl acetate in hexane). MS (CI, CH4) m/z 561 (M+1,100), 563 (40), 589 (M+29,20), 545 (26), 429 (26)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681840
Source datasetuspto-grants-1997_10
ORD IDord-6663f6e7b56e4e42b665204d66d86f67
Source noteuspto-grants-1997_10