HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Tert-butyl 7-hydroxychromane-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | tert-butyl 7-(benzyloxy)-2H-chromene-3-carboxylate | HCID 59832107 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 7-hydroxychromane-3-carboxylate | HCID 59832111 | 62.4% |
Reaction Steps
tert-butyl 7-(benzyloxy)-2H-chromene-3-carboxylate (13 g) was dissolved in ethyl acetate (15 ml) and methanol (5 ml) in a hydrogenation bottle. Pd—C (10%) (1 g) was added and the reaction mixture was hydrogenated (H2, 70 psi & RT) for overnight. After the completion of the reaction, catalyst was filtered and washed with 100 ml of ethyl acetate. Solvent was evaporated and the crude product was purified using column chromatography and ethyl acetate hexane mixture to give 6 g of pure product (48.3% overall for 2 steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446127B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-8009cfed7c53423b9bac49313e0f3271 |
| Source note | uspto-grants-2008_11 |