HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 19922465, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15296109 | HCID 15296109 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19922465 | HCID 19922465 | — |
Reaction Steps
To 300 mg of 9,9-bis(4-pyridinylmethyl)-2-acetylfluorene was dissolved in 5 ml of ethanol cooled to 0° was added 100 mg of sodium borohydride. The reaction mixture was warmed to room temperature overnight, quenched with water and methanol and the solvents evaporated. The residue was partitioned between ethyl acetate and 1N NaOH, washed with water, brine, dried (MgSO4) and evaporated. Recrystallization from ethanol yielded product. NMR (CDCl3, 200 MHz) δ: 1.50(d,J=6.5 Hz, 3H), 3.39(s,4H), 4.92(q,J=6.4 Hz, 1H), 6.43(2d,4H), 7.08-7.58(m, arom.), 7.87(d,2H), 7.97(d,2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05300642 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-97640bc2cd3b499fa415feea7fc26217 |
| Source note | uspto-grants-1994_04 |