HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → [5-(3-Bromophenylsulphanylmethyl)-2-hydroxymethylphenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Dimethyl 4-(3-bromophenylsulphanylmethyl)phthalate | HCID 22606944 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [5-(3-Bromophenylsulphanylmethyl)-2-hydroxymethylphenyl]methanol | HCID 22606907 | — |
Reaction Steps
Dimethyl 4-(3-bromophenylsulphanylmethyl)phthalate (10 g, 26 mmol) is dissolved in 120 mL of anhydrous THF. 2.2 g of lithium borohydride (100 mmol) are then added slowly, after which the reaction medium is refluxed for 12 h. After cooling and treatment with saturated ammonium chloride solution, the reaction medium is extracted with ethyl acetate. The organic phases are combined, dried and concentrated under reduced pressure. The residue is purified by chromatography on a column of silica, to give a colourless oil (7.8 g, Y=89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06831106B1 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-c5ff1e6233414a4fa92a1d072ca923e8 |
| Source note | uspto-grants-2004_12 |