HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 14990561, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14990560 | HCID 14990560 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14990561 | HCID 14990561 | 62.5% |
Reaction Steps
To a stirred solution of 17 parts of (4-fluorophenyl) [1-(1-methylethyl)-1H-benzotriazol-5-yl]methanone in 80 parts of ethanol were added 3.4 parts of sodium tetrahydroborate. After stirring for 1 hour at room temperature, the reaction mixture was neutralized to pH 7. The reaction mixture was concentrated and the product was extracted with ethyl acetate. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 10.7 parts (62.5%) of α-(4-fluorophenyl)-1-(1-methylethyl)-1H-benzotriazole-5-methanol as a residue (int. 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04943574 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-488be89842b74e2db449cbbae8f9921f |
| Source note | uspto-grants-1990_07 |