HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl 5-butoxyisophthalate → (3-Butoxy-5-hydroxymethyl-phenyl)-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl 5-butoxyisophthalate | HCID 18667930 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Butoxy-5-hydroxymethyl-phenyl)-methanol | HCID 57443335 | 60.1% |
Reaction Steps
To a solution of dimethyl 5-butoxyisophthalate (0.51 g, 1.90 mmol) in THF (16 mL) was slowly added LiAlH4 (0.40 g, 10.5 mmol). The reaction mixture was stirred for 8 h. The reaction was quenched by the addition of 2N aq. HCl (5 mL). The mixture was extracted with Et2O (2×25 mL) and EtOAc (2×25 mL), the organics layers combined, dried over Na2SO4, filtered, and concentrated under reduced pressure to afford the desired product (0.24 g) as an oil, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09439433B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-31b6da7972c84e80a6fc41a44c88dc8c |
| Source note | uspto-grants-2016_09 |