HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyltributylstannane → HCID 54040908, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyltributylstannane | HCID 90628 | — |
| Reactant | (4aR)-(10bR)-4,10b-dimethyl-8-bromo-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one | HCID 15355317 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54040908 | HCID 54040908 | — |
Reaction Steps
A 9 g portion of (4aR)-(10bR)-4,10b-dimethyl-8-bromo-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one was combined with 11.1 g of tri-n-butyl-2-propenylstannane and 1.69 g of tetrakis(triphenylphosphene) palladium in 40 mL of acetonitrile in a sealable tube. Argon was bubbled through the mixture, the cap replaced, and the reaction heated at 90° for 18 h. Upon cooling, the mixture was filtered and the filtrate was concentrated under vacuum. The residue was triturated with diethyl ether to obtain 4.23 g of crystalline product, and a second crop of 1.31 g of product was also obtained. mp 144°-146°; FDMS 255M+; Calcd for C17H21N1O2 :
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05629007 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-3e6e3e484f374611a49e41970669fbf2 |
| Source note | uspto-grants-1997_05 |