HuagongsheHuagongshe Chemistry Print Report · For research reference only
(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinone → HCID 21480638, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinone | HCID 21480605 | — |
| Reactant | 3-Bromo-5-(((tert-butyldimethylsilyl)oxy)methyl)pyridine | HCID 21984091 | — |
| Product | HCID 21480638 | HCID 21480638 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05681840 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-50c564206002423aa7d10a802cfedd1a |
| Source note | uspto-grants-1997_10 |