HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → (+/-)-4-[[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl](phenylmethyl) amino]-butanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | Benzyl-chroman-2-ylmethyl-amine; oxalic acid | HCID 10753388 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (+/-)-4-[[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl](phenylmethyl) amino]-butanenitrile | HCID 21460889 | 69.6% |
Reaction Steps
A mixture of 12.5 g of 3,4-dihydro-N-(phenylmethyl)-2H-1-benzopyran-2-methanamine, 9 g of 4-bromobutanenitrile, 200 ml of N,N-dimethylformamide and 10 ml of N,N-diethylethanamine was stirred for 72 hour at room temperature. The reaction mixture was evaporated and the residue was partitioned between 1,1'-oxybisethane and water. The organic layer was separated, dried, filtered and evaporated, yielding 11 g (68.7 % ) of (±)-4-[[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl](phenylmethyl)amino]butanenitrile (interm. 53).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688952 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-812e723512204febaaecab8b437df3fe |
| Source note | uspto-grants-1997_11 |