HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 19689353, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Chloro-4'-trifluoromethylsulfonylmethylbenzophenone | HCID 11132212 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19689353 | HCID 19689353 | 77% |
Reaction Steps
4-chloro-4'-trifluoromethylsulfonylmethylbenzophenone (5.5 g) was dispersed in methanol (200 ml). Sodium borohydride was gradually added thereto at room temperature with stirring, and the mixture was further stirred overnight at room temperature. After completion of the reaction, methanol was distilled off under reduced pressure. The residue was extracted with ethyl acetate (250 ml). The extract was washed with water and dried over anhydrous magnesium sulfate. Then, ethyl acetate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=2:1) to obtain the desired product as a white powder (4.2 g, melting point: 113° to 115° C., yield: 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728699 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-0d7170f4c2ba43dc88cc7ef00696f625 |
| Source note | uspto-grants-1998_03 |