HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-5-methoxybenzoic acid → (3-Chloro-5-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-5-methoxybenzoic acid | HCID 12909341 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Chloro-5-methoxyphenyl)methanol | HCID 12909342 | 101.5% |
Reaction Steps
Lithium aluminium hydride (1M in THF, 8.76 ml) was added dropwise to a stirred solution of the product of step (i) (1.63 g) in THF (40 ml) and stirred for 2 h. The reaction was diluted with 2 M HCl and extracted with ethyl acetate. The organic layer was washed with aqueous sodium hydrogen carbonate, dried (MgSO4) and evaporated under reduced pressure to give the subtitle compound (1.53 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08148572B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-313491dc57df4c8b8525158585c47432 |
| Source note | uspto-grants-2012_04 |