HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium fluoride → Methyl 5-hydroxy-2-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium fluoride | HCID 25516 | — |
| Reactant | Methyl 2-methoxy-5-(t-butyldimethylsilyloxy)benzoate | HCID 18464864 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-hydroxy-2-methoxybenzoate | HCID 592162 | — |
Reaction Steps
Combine methyl 2-methoxy-5-(t-butyldimethylsilyloxy)benzoate (11.1 g. 37.4 mmol) and ammonium fluoride (6.94 g, 0.187 mmol) in methanol (150 mL). Heat to reflux. After 1 hour, evaporate in vacuo to give a residue. Partition the residue between ethyl acetate and water, separate the layers, extract the organic layer with water and then brine. Dry the organic layer over MgSO4, filter, and evaporate in uacuo to give methyl 2-methoxy-5-hydroxybenzoate: mp; 110-112° C. Rf=0.27 (silica gel, 5% ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194406B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-cc63f7f2d2c947808406a91e56a6584e |
| Source note | uspto-grants-2001_02 |